| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001029869.1 | 467 | Missense Mutation | TGT,TTT | C109F | NP_001025040.1 |
| XM_005268381.3 | 467 | Missense Mutation | TGT,TTT | C89F | XP_005268438.1 |
| XM_011537571.2 | 467 | Missense Mutation | TGT,TTT | C82F | XP_011535873.1 |
| XM_017009137.1 | 467 | Missense Mutation | TGT,TTT | C82F | XP_016864626.1 |