Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001300814.1 | 827 | Missense Mutation | CCG,CTG | P272L | NP_001287743.1 |
NM_173352.3 | 827 | Missense Mutation | CCG,CTG | P382L | NP_775487.2 |
XM_011538010.1 | 827 | Missense Mutation | CCG,CTG | P350L | XP_011536312.1 |