Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001039775.3 | 4770 | Missense Mutation | CCG,CTG | P1545L | NP_001034864.2 |
XM_005245918.2 | 4770 | Missense Mutation | CCG,CTG | P1545L | XP_005245975.1 |
XM_011541672.1 | 4770 | Missense Mutation | CCG,CTG | P1533L | XP_011539974.1 |
XM_011541673.2 | 4770 | Missense Mutation | CCG,CTG | P1602L | XP_011539975.1 |