| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001243224.1 | 615 | Missense Mutation | CGG,TGG | R28W | NP_001230153.1 |
| NM_004584.2 | 615 | Missense Mutation | CGG,TGG | R104W | NP_004575.1 |
| XM_006718652.3 | 615 | Missense Mutation | CGG,TGG | R115W | XP_006718715.1 |
| XM_017018097.1 | 615 | Silent Mutation | GCC,GCT | A2A | XP_016873586.1 |
| XM_017018098.1 | 615 | UTR 5 | XP_016873587.1 |