Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001029885.1 | 774 | Missense Mutation | CCG,CTG | P120L | NP_001025056.1 |
XM_005244801.3 | 774 | Missense Mutation | CCG,CTG | P120L | XP_005244858.1 |
XM_005244802.1 | 774 | Missense Mutation | CCG,CTG | P57L | XP_005244859.1 |
XM_011542200.2 | 774 | Missense Mutation | CCG,CTG | P120L | XP_011540502.1 |