Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001001991.2 | 2518 | Missense Mutation | CCG,CTG | P674L | NP_001001991.1 |
NM_001282675.1 | 2518 | Missense Mutation | CCG,CTG | P634L | NP_001269604.1 |
NM_001282676.1 | 2518 | Missense Mutation | CCG,CTG | P563L | NP_001269605.1 |
NM_015430.3 | 2518 | Missense Mutation | CCG,CTG | P691L | NP_056245.2 |