| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001195833.1 | 938 | Missense Mutation | GCC,GTC | A286V | NP_001182762.1 |
| NM_198445.3 | 938 | Intron | NP_940847.1 | ||
| XM_006723015.2 | 938 | Missense Mutation | GCC,GTC | A286V | XP_006723078.1 |
| XM_006723016.2 | 938 | Missense Mutation | GCC,GTC | A172V | XP_006723079.1 |
| XM_011526454.2 | 938 | Missense Mutation | GCC,GTC | A286V | XP_011524756.1 |
| XM_011526455.2 | 938 | Intron | XP_011524757.1 |