| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001304535.1 | 780 | Intron | NP_001291464.1 | ||
| NM_175911.3 | 780 | Intron | NP_787107.1 | ||
| XM_011544169.2 | 780 | Intron | XP_011542471.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001004686.2 | 780 | Missense Mutation | ACG,ATG | T185M | NP_001004686.1 |
| XM_011544158.2 | 780 | Missense Mutation | ACG,ATG | T185M | XP_011542460.1 |