| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001258390.1 | 460 | Missense Mutation | CGG,TGG | R42W | NP_001245319.1 |
| NM_001258391.1 | 460 | UTR 5 | NP_001245320.1 | ||
| NM_001318799.1 | 460 | UTR 5 | NP_001305728.1 | ||
| NM_178834.4 | 460 | Missense Mutation | CGG,TGG | R34W | NP_849156.1 |
| XM_006718769.3 | 460 | UTR 5 | XP_006718832.1 | ||
| XM_006718770.3 | 460 | UTR 5 | XP_006718833.1 |