| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001199085.1 | 669 | Missense Mutation | CGG,TGG | R51W | NP_001186014.1 |
| NM_001199089.1 | 669 | Missense Mutation | CGG,TGG | R51W | NP_001186018.1 |
| NM_001199091.1 | 669 | Missense Mutation | CGG,TGG | R51W | NP_001186020.1 |
| NM_001199092.1 | 669 | Intron | NP_001186021.1 | ||
| NM_173533.3 | 669 | Missense Mutation | CGG,TGG | R51W | NP_775804.2 |
| XM_005244934.1 | 669 | Missense Mutation | CGG,TGG | R51W | XP_005244991.1 |
| XM_005244935.4 | 669 | Missense Mutation | CGG,TGG | R51W | XP_005244992.1 |
| XM_017000473.1 | 669 | Missense Mutation | CGG,TGG | R51W | XP_016855962.1 |