| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001001715.3 | 449 | Intron | NP_001001715.2 | ||
| NM_001286839.1 | 449 | Intron | NP_001273768.1 | ||
| NM_005766.3 | 449 | Intron | NP_005757.1 | ||
| XM_011521046.2 | 449 | Intron | XP_011519348.1 | ||
| XM_017020312.1 | 449 | Intron | XP_016875801.1 | ||
| XM_017020313.1 | 449 | Intron | XP_016875802.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_178861.4 | 449 | Missense Mutation | GGT,TGT | G140C | NP_849192.1 |