Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_183062.2 | 182 | Missense Mutation | CCG,CTG | P61L | NP_898885.1 |
XM_011544175.2 | 182 | Missense Mutation | CCG,CTG | P61L | XP_011542477.1 |
XM_011544176.2 | 182 | Missense Mutation | CCG,CTG | P61L | XP_011542478.1 |