Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001040708.1 | 697 | Missense Mutation | CCG,CTG | P256L | NP_001035798.1 |
NM_001282851.1 | 697 | Missense Mutation | CCG,CTG | P162L | NP_001269780.1 |
NM_012258.3 | 697 | Missense Mutation | CCG,CTG | P252L | NP_036390.3 |