| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001272087.1 | 1764 | Intron | NP_001259016.1 | ||
| NM_001272088.1 | 1764 | Intron | NP_001259017.1 | ||
| NM_005071.2 | 1764 | Missense Mutation | CGG,TGG | R525W | NP_005062.1 |
| XM_006722842.1 | 1764 | Missense Mutation | CGG,TGG | R525W | XP_006722905.1 |
| XM_006722844.1 | 1764 | Missense Mutation | CGG,TGG | R525W | XP_006722907.1 |
| XM_017027152.1 | 1764 | Missense Mutation | CGG,TGG | R525W | XP_016882641.1 |