| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001305141.1 | 1177 | Missense Mutation | TGC,TGG | C288W | NP_001292070.1 |
| NM_001305142.1 | 1177 | Missense Mutation | TGC,TGG | C288W | NP_001292071.1 |
| NM_020677.4 | 1177 | Missense Mutation | TGC,TGG | C288W | NP_065728.1 |
| XM_006720905.3 | 1177 | Missense Mutation | TGC,TGG | C225W | XP_006720968.1 |
| XM_006720906.2 | 1177 | Missense Mutation | TGC,TGG | C224W | XP_006720969.1 |
| XM_011522567.2 | 1177 | Intron | XP_011520869.1 | ||
| XM_017023485.1 | 1177 | Missense Mutation | TGC,TGG | C324W | XP_016878974.1 |
| XM_017023486.1 | 1177 | Intron | XP_016878975.1 | ||
| XM_017023487.1 | 1177 | Intron | XP_016878976.1 | ||
| XM_017023488.1 | 1177 | Intron | XP_016878977.1 | ||
| XM_017023489.1 | 1177 | Missense Mutation | TGC,TGG | C224W | XP_016878978.1 |
| XM_017023490.1 | 1177 | Missense Mutation | TGC,TGG | C225W | XP_016878979.1 |
| XM_017023491.1 | 1177 | UTR 3 | XP_016878980.1 | ||
| XM_017023492.1 | 1177 | UTR 3 | XP_016878981.1 |