Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001256119.1 | 813 | Missense Mutation | CCG,CTG | P173L | NP_001243048.1 |
NM_001256120.1 | 813 | Missense Mutation | CCG,CTG | P182L | NP_001243049.1 |
NM_003491.3 | 813 | Missense Mutation | CCG,CTG | P188L | NP_003482.1 |