| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001136019.2 | 676 | Missense Mutation | GGG,TGG | G152W | NP_001129491.1 |
| NM_004107.4 | 676 | Missense Mutation | GGG,TGG | G152W | NP_004098.1 |
| XM_005258657.1 | 676 | Missense Mutation | GGG,TGG | G12W | XP_005258714.1 |
| XM_011526627.2 | 676 | Intron | XP_011524929.1 |