| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001122870.2 | 645 | Missense Mutation | CGG,TGG | R30W | NP_001116342.1 |
| NM_144641.3 | 645 | Missense Mutation | CGG,TGG | R242W | NP_653242.3 |
| XM_005264879.2 | 645 | Missense Mutation | CGG,TGG | R242W | XP_005264936.1 |
| XM_005264880.3 | 645 | Missense Mutation | CGG,TGG | R157W | XP_005264937.1 |
| XM_005264881.1 | 645 | Missense Mutation | CGG,TGG | R81W | XP_005264938.1 |