ID: 5691 | proteasome 20S subunit beta 3 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38752741..38764225) | HC10-II | 602176 |
ID: 5546 | proline rich mitotic checkpoint control factor [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (156767535..156800815) | RCCP1, TPRC | 179755 |
ID: 55017 | chromosome 14 open reading frame 119 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (23095505..23100456) | | |
ID: 23197 | Fas associated factor family member 2 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (176448385..176510074) | ETEA, UBXD8, UBXN3B | 616935 |
ID: 10621 | RNA polymerase III subunit F [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (18467390..18484646) | C34, IMD101, RPC39, RPC6 | 617455 |
ID: 5936 | RNA binding motif protein 4 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66638703..66668380) | LARKA, ZCCHC21, ZCRB3A, RBM4 | 602571 |
ID: 81857 | mediator complex subunit 25 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49818289..49840384) | ACID1, ARC92, BVSYS, CMT2B2, P78, PTOV2, TCBAP0758 | 610197 |
ID: 3133 | major histocompatibility complex, class I, E [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (30489509..30494194) | HLA-6.2, QA1 | 143010 |
ID: 54957 | thioredoxin like 4B [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (72084857..72094378, complement) | DLP, Dim2 | 617722 |
ID: 6832 | Suv3 like RNA helicase [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (69180234..69209093) | SUV3 | 605122 |
ID: 55676 | solute carrier family 30 member 6 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (32165864..32224379) | MST103, MSTP103, ZNT6 | 611148 |
ID: 7700 | zinc finger protein 141 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (337814..384868) | D4S90, pHZ-44 | 194648 |
ID: 28956 | late endosomal/lysosomal adaptor, MAPK and MTOR activator 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (156054782..156058506) | ENDAP, HSPC003, MAPBPIP, MAPKSP1AP, ROBLD3, Ragulator2, p14 | 610389 |
ID: 10428 | craniofacial development protein 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (75293710..75433503, complement) | BCNT, BUCENTAUR, CENP-29, CP27, SWC5, Yeti, p97 | 608108 |
ID: 4548 | 5-methyltetrahydrofolate-homocysteine methyltransferase [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (236795281..236903981) | HMAG, MS, cblG | 156570 |