| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001321163.1 | 1012 | Intron | NP_001308092.1 | ||
| NM_021915.3 | 1012 | Intron | NP_068734.1 | ||
| XM_006722873.3 | 1012 | Intron | XP_006722936.1 | ||
| XM_006722874.3 | 1012 | Intron | XP_006722937.1 | ||
| XM_017027231.1 | 1012 | Intron | XP_016882720.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001271848.1 | 1012 | Missense Mutation | TGT,TTT | C290F | NP_001258777.1 |
| NM_144566.2 | 1012 | Missense Mutation | TGT,TTT | C287F | NP_653167.1 |