| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001256841.1 | 357 | Missense Mutation | CGG,TGG | R5W | NP_001243770.1 |
| NM_007261.3 | 357 | Missense Mutation | CGG,TGG | R5W | NP_009192.2 |
| XM_005256990.2 | 357 | Missense Mutation | CGG,TGG | R5W | XP_005257047.1 |
| XM_005256991.4 | 357 | Missense Mutation | CGG,TGG | R5W | XP_005257048.1 |
| XM_005256992.4 | 357 | Intron | XP_005257049.1 | ||
| XM_006721656.3 | 357 | Intron | XP_006721719.1 | ||
| XM_011524254.2 | 357 | Missense Mutation | CGG,TGG | R5W | XP_011522556.1 |