Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001311311.1 | 686 | Missense Mutation | CCG,CTG | P139L | NP_001298240.1 |
NM_024006.5 | 686 | Missense Mutation | CCG,CTG | P111L | NP_076869.1 |
NM_206824.2 | 686 | Silent Mutation | CCC,CCT | P74P | NP_996560.1 |