ID: 6506 | solute carrier family 1 member 2 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (35251205..35420507, complement) | DEE41, EAAT2, EIEE41, GLT-1, GLT1, HBGT | 600300 |
ID: 6505 | solute carrier family 1 member 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (4490468..4587469) | DCBXA, EAAC1, EAAT3, SCZD18, hEAAC1 | 133550 |
ID: 6507 | solute carrier family 1 member 3 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (36606606..36688334) | EA6, EAAT1, GLAST, GLAST1 | 600111 |
ID: 6531 | solute carrier family 6 member 3 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (1392794..1445440, complement) | DAT, DAT1, PKDYS, PKDYS1 | 126455 |
ID: 23657 | solute carrier family 7 member 11 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (138164097..138312671, complement) | CCBR1, xCT | 607933 |
ID: 6510 | solute carrier family 1 member 5 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (46774883..46788594, complement) | AAAT, ASCT2, ATBO, M7V1, M7VS1, R16, RDRC | 109190 |
ID: 57030 | solute carrier family 17 member 7 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49429401..49441527, complement) | BNPI, VGLUT1 | 605208 |
ID: 57084 | solute carrier family 17 member 6 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (22338381..22379503) | DNPI, VGLUT2 | 607563 |
ID: 6568 | solute carrier family 17 member 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (25723743..25832052, complement) | NAPI-1, NPT-1, NPT1 | 182308 |
ID: 246213 | solute carrier family 17 member 8 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (100357074..100422055) | DFNA25, VGLUT3 | 607557 |
ID: 26503 | solute carrier family 17 member 5 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (73593379..73653992, complement) | AST, ISSD, NSD, SD, SIALIN, SIASD, SLD, VEAT | 604322 |
ID: 6511 | solute carrier family 1 member 6 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (14950033..15010643, complement) | EAAT4 | 600637 |
ID: 6512 | solute carrier family 1 member 7 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (53087183..53142638, complement) | AAAT, EAAT5 | 604471 |
ID: 157724 | solute carrier family 7 member 13 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (86214063..86230381, complement) | AGT-1, AGT1, XAT2 | 617256 |
ID: 79751 | solute carrier family 25 member 22 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (790475..798281, complement) | DEE3, EIEE3, GC-1, GC1, NET44 | 609302 |
ID: 10246 | solute carrier family 17 member 2 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (25912754..25930691, complement) | NPT3 | 611049 |
ID: 140679 | solute carrier family 32 member 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (38724486..38729372) | DEE114, GEFSP12, VGAT, VIAAT, VIAAT GEFSP12 | 616440 |
ID: 7157 | tumor protein p53 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7668421..7687490, complement) | BCC7, BMFS5, LFS1, P53, TRP53 | 191170 |
ID: 27670601 | solute carrier family 25 (mitochondrial aspartate/glutamate transporter), member 12/13 [Sporothrix schenckii 1099-18] | | SPSK_08736 | |
ID: 88179590 | solute carrier family 25 (mitochondrial aspartate/glutamate transporter) member 12/13 [Cryptococcus deuterogattii R265] | Chromosome 1, NC_086139.1 (1062421..1065826) | CNBG_3296 | |