| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001178145.1 | 8627 | Silent Mutation | ACA,ACG | T633T | NP_001171616.1 |
| NM_001178146.1 | 8627 | Silent Mutation | ACA,ACG | T585T | NP_001171617.1 |
| NM_178822.4 | 8627 | Silent Mutation | ACA,ACG | T2606T | NP_849144.2 |
| XM_011512708.2 | 8627 | Silent Mutation | ACA,ACG | T2678T | XP_011511010.1 |
| XM_011512709.2 | 8627 | Silent Mutation | ACA,ACG | T2606T | XP_011511011.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_053002.5 | 8627 | Intron | NP_443728.3 | ||
| XM_006713487.3 | 8627 | Intron | XP_006713550.1 | ||
| XM_011512390.2 | 8627 | Intron | XP_011510692.1 | ||
| XM_011512394.2 | 8627 | Intron | XP_011510696.1 | ||
| XM_011512399.2 | 8627 | Intron | XP_011510701.1 | ||
| XM_017005676.1 | 8627 | Intron | XP_016861165.1 | ||
| XM_017005677.1 | 8627 | Intron | XP_016861166.1 | ||
| XM_017005678.1 | 8627 | Intron | XP_016861167.1 | ||
| XM_017005679.1 | 8627 | Intron | XP_016861168.1 | ||
| XM_017005680.1 | 8627 | Intron | XP_016861169.1 | ||
| XM_017005681.1 | 8627 | Intron | XP_016861170.1 |