Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001080462.1 | 170 | Missense Mutation | CAA,CGA | Q57R | NP_001073931.1 |
XM_011521497.1 | 170 | Missense Mutation | CAA,CGA | Q18R | XP_011519799.1 |
XM_011521499.1 | 170 | Intron | XP_011519801.1 |