Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_012448.3 | 2312 | Missense Mutation | CAG,CGG | Q775R | NP_036580.2 |
XM_005257626.4 | 2312 | Intron | XP_005257683.1 | ||
XM_017024977.1 | 2312 | Missense Mutation | CAG,CGG | Q681R | XP_016880466.1 |