| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001145444.1 | 3499 | Missense Mutation | CGG,TGG | R1025W | NP_001138916.1 |
| NM_001145445.1 | 3499 | Missense Mutation | CGG,TGG | R1018W | NP_001138917.1 |
| NM_020706.2 | 3499 | Missense Mutation | CGG,TGG | R1040W | NP_065757.1 |
| XM_005261017.2 | 3499 | Missense Mutation | CGG,TGG | R981W | XP_005261074.1 |
| XM_006724035.2 | 3499 | Missense Mutation | CGG,TGG | R1036W | XP_006724098.1 |
| XM_006724036.2 | 3499 | Missense Mutation | CGG,TGG | R1014W | XP_006724099.1 |
| XM_017028415.1 | 3499 | Missense Mutation | CGG,TGG | R1039W | XP_016883904.1 |
| XM_017028416.1 | 3499 | Missense Mutation | CGG,TGG | R1017W | XP_016883905.1 |
| XM_017028417.1 | 3499 | Missense Mutation | CGG,TGG | R959W | XP_016883906.1 |