HapMap
HapMap
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000962.3 | 328 | Missense Mutation | CGG,TGG | R8W | NP_000953.2 |
| NM_001271164.1 | 328 | Missense Mutation | CGG,TGG | R8W | NP_001258093.1 |
| NM_001271165.1 | 328 | Intron | NP_001258094.1 | ||
| NM_001271166.1 | 328 | UTR 5 | NP_001258095.1 | ||
| NM_001271367.1 | 328 | UTR 5 | NP_001258296.1 | ||
| NM_001271368.1 | 328 | UTR 5 | NP_001258297.1 | ||
| NM_080591.2 | 328 | Missense Mutation | CGG,TGG | R8W | NP_542158.1 |
| XM_005252105.3 | 328 | UTR 5 | XP_005252162.1 | ||
| XM_011518875.2 | 328 | UTR 5 | XP_011517177.1 | ||
| XM_011518876.2 | 328 | UTR 5 | XP_011517178.1 | ||
| XM_017014929.1 | 328 | UTR 5 | XP_016870418.1 |