| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001304441.1 | 1486 | Missense Mutation | GCC,GTC | A413V | NP_001291370.1 |
| NM_001304442.1 | 1486 | Missense Mutation | GCC,GTC | A413V | NP_001291371.1 |
| NM_002424.2 | 1486 | Missense Mutation | GCC,GTC | A436V | NP_002415.1 |
| XM_011542834.2 | 1486 | Missense Mutation | GCC,GTC | A445V | XP_011541136.1 |
| XM_011542835.2 | 1486 | Missense Mutation | GCC,GTC | A413V | XP_011541137.1 |
| XM_011542836.2 | 1486 | UTR 3 | XP_011541138.1 | ||
| XM_017017771.1 | 1486 | Missense Mutation | GCC,GTC | A413V | XP_016873260.1 |