Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_031421.3 | 442 | Missense Mutation | CAG,CGG | Q114R | NP_113609.1 |
XM_011525323.2 | 442 | Intron | XP_011523625.1 | ||
XM_011525324.2 | 442 | Missense Mutation | CAG,CGG | Q114R | XP_011523626.1 |