Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001079839.2 | 446 | Missense Mutation | ACG,CCG | T10P | NP_001073308.1 |
NM_001079840.2 | 446 | Missense Mutation | ACG,CCG | T10P | NP_001073309.1 |
NM_001079841.2 | 446 | Missense Mutation | ACG,CCG | T10P | NP_001073310.1 |
NM_001079842.2 | 446 | Missense Mutation | ACG,CCG | T10P | NP_001073311.2 |
NM_001168254.1 | 446 | Missense Mutation | ACG,CCG | T15P | NP_001161726.1 |
NM_017830.3 | 446 | Missense Mutation | ACG,CCG | T10P | NP_060300.1 |
XM_017008329.1 | 446 | Missense Mutation | ACG,CCG | T10P | XP_016863818.1 |