Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_152397.2 | 466 | Missense Mutation | CAG,CGG | Q123R | NP_689610.2 |
XM_011533366.2 | 466 | Missense Mutation | CAG,CGG | Q88R | XP_011531668.1 |
XM_017005729.1 | 466 | Missense Mutation | CAG,CGG | Q88R | XP_016861218.1 |