Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001127266.1 | 1242 | Missense Mutation | CAG,CGG | Q241R | NP_001120738.1 |
NM_138385.3 | 1242 | Intron | NP_612394.1 | ||
XM_005248038.4 | 1242 | Missense Mutation | CAG,CGG | Q168R | XP_005248095.1 |
XM_005248039.4 | 1242 | Missense Mutation | CAG,CGG | Q168R | XP_005248096.1 |
XM_011513594.2 | 1242 | Missense Mutation | CAG,CGG | Q168R | XP_011511896.1 |
XM_017008834.1 | 1242 | Missense Mutation | CAG,CGG | Q168R | XP_016864323.1 |