| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001320865.1 | 61 | Missense Mutation | GCC,GGC | A11G | NP_001307794.1 |
| NM_198559.1 | 61 | Intron | NP_940961.1 | ||
| XM_005246539.4 | 61 | Intron | XP_005246596.1 | ||
| XM_005246541.4 | 61 | Intron | XP_005246598.1 | ||
| XM_011511148.2 | 61 | Missense Mutation | GCC,GGC | A11G | XP_011509450.1 |
| XM_011511149.2 | 61 | Intron | XP_011509451.1 | ||
| XM_011511150.2 | 61 | Intron | XP_011509452.1 | ||
| XM_017004053.1 | 61 | Intron | XP_016859542.1 |