Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_173821.2 | 202 | Missense Mutation | CCG,CTG | P60L | NP_776182.2 |
XM_011510995.2 | 202 | Missense Mutation | CCG,CTG | P39L | XP_011509297.1 |
XM_011510997.2 | 202 | Missense Mutation | CCG,CTG | P60L | XP_011509299.1 |