Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001204872.1 | 523 | Missense Mutation | CCG,CTG | P134L | NP_001191801.1 |
NM_001204873.1 | 523 | Missense Mutation | CCG,CTG | P114L | NP_001191802.1 |
NM_024663.3 | 523 | Missense Mutation | CCG,CTG | P162L | NP_078939.3 |