| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000087.3 | 1645 | Missense Mutation | GGG,TGG | G442W | NP_000078.2 |
| NM_001142564.1 | 1645 | Missense Mutation | GGG,TGG | G511W | NP_001136036.1 |
| XM_005248049.4 | 1645 | Missense Mutation | GGG,TGG | G517W | XP_005248106.2 |
| XM_011513623.2 | 1645 | Missense Mutation | GGG,TGG | G442W | XP_011511925.1 |
| XM_017007712.1 | 1645 | Missense Mutation | GGG,TGG | G442W | XP_016863201.1 |