| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001031722.3 | 298 | Missense Mutation | GCC,GTC | A73V | NP_001026892.1 |
| NM_001190724.2 | 298 | Missense Mutation | GCC,GTC | A73V | NP_001177653.1 |
| NM_001254952.2 | 298 | Missense Mutation | GCC,GTC | A85V | NP_001241881.1 |
| NM_001318762.1 | 298 | Missense Mutation | GCC,GTC | A85V | NP_001305691.1 |
| NM_001318763.1 | 298 | Missense Mutation | GCC,GTC | A85V | NP_001305692.1 |
| NM_024909.3 | 298 | Missense Mutation | GCC,GTC | A85V | NP_079185.2 |
| XM_005249415.2 | 298 | Missense Mutation | GCC,GTC | A73V | XP_005249472.1 |
| XM_011514918.2 | 298 | Intron | XP_011513220.1 | ||
| XM_017011316.1 | 298 | Missense Mutation | GCC,GTC | A73V | XP_016866805.1 |