ID: 9751 | syntaphilin [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (1266294..1309327) | | 604942 |
ID: 5566 | protein kinase cAMP-activated catalytic subunit alpha [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (14091688..14117762, complement) | CAFD1, PKACA, PPNAD4 | 601639 |
ID: 10273 | STIP1 homology and U-box containing protein 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (680410..682801) | CHIP, HSPABP2, NY-CO-7, SCA48, SCAR16, SDCCAG7, UBOX1 | 607207 |
ID: 7874 | ubiquitin specific peptidase 7 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (8892097..8963906, complement) | C16DELp13.2, DEL16P13.2, HAFOUS, HAUSP, TEF1 | 602519 |
ID: 10381 | tubulin beta 3 class III [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89921925..89936097) | CDCBM, CDCBM1, CFEOM3, CFEOM3A, FEOM3, TUBB4, beta-4 | 602661 |
ID: 7507 | XPA, DNA damage recognition and repair factor [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (97654398..97697340, complement) | XP1C, XPA | 611153 |
ID: 6804 | syntaxin 1A [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (73699210..73719669, complement) | HPC-1, P35-1, STX1, SYN1A | 186590 |
ID: 3796 | kinesin family member 2A [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (62306206..62391025) | CDCBM3, HK2, KIF2 | 602591 |
ID: 25962 | vir like m6A methyltransferase associated [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (94487689..94553469, complement) | KIAA1429, MSTP054, fSAP121 | 616447 |
ID: 23332 | cytoplasmic linker associated protein 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (121337776..121649462, complement) | MAST1 | 605852 |
ID: 51606 | ATPase H+ transporting V1 subunit H [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (53715543..53843245, complement) | CGI-11, MSTP042, NBP1, SFD, SFDalpha, SFDbeta, VMA13 | 608861 |
ID: 23363 | obscurin like cytoskeletal adaptor 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (219547206..219571539, complement) | | 610991 |
ID: 57414 | rhomboid domain containing 2 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (75879034..75888926) | NPD007, RHBDL7 | 615203 |
ID: 55638 | syntabulin [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (109573978..109691600, complement) | GOLSYN, OCSYN, SNPHL | 611568 |