| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001031684.2 | 496 | Missense Mutation | CGG,TGG | R131W | NP_001026854.1 |
| NM_001195446.1 | 496 | Missense Mutation | CGG,TGG | R131W | NP_001182375.1 |
| XM_005264484.2 | 496 | Missense Mutation | CGG,TGG | R131W | XP_005264541.1 |
| XM_005264485.2 | 496 | Missense Mutation | CGG,TGG | R131W | XP_005264542.1 |
| XM_011533032.2 | 496 | Missense Mutation | CGG,TGG | R14W | XP_011531334.1 |