Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001014987.1 | 597 | Missense Mutation | CCA,CTA | P82L | NP_001014987.1 |
NM_001014988.1 | 597 | Missense Mutation | CCA,CTA | P82L | NP_001014988.1 |
NM_001014989.1 | 597 | Missense Mutation | CCA,CTA | P118L | NP_001014989.2 |
NM_014387.3 | 597 | Missense Mutation | CCA,CTA | P82L | NP_055202.1 |