Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001304284.1 | 2654 | Missense Mutation | CAG,CGG | Q69R | NP_001291213.1 |
NM_004505.3 | 2654 | Intron | NP_004496.2 | ||
XM_011524050.1 | 2654 | Missense Mutation | CAG,CGG | Q69R | XP_011522352.1 |
XM_011524051.2 | 2654 | Missense Mutation | CAG,CGG | Q69R | XP_011522353.1 |
XM_011524052.2 | 2654 | Intron | XP_011522354.1 | ||
XM_011524053.2 | 2654 | Intron | XP_011522355.1 | ||
XM_011524054.2 | 2654 | Missense Mutation | CAG,CGG | Q69R | XP_011522356.1 |
XM_011524055.2 | 2654 | Missense Mutation | CAG,CGG | Q69R | XP_011522357.1 |
XM_011524056.2 | 2654 | Intron | XP_011522358.1 | ||
XM_011524057.2 | 2654 | Missense Mutation | CAG,CGG | Q69R | XP_011522359.1 |
XM_011524058.2 | 2654 | Missense Mutation | CAG,CGG | Q69R | XP_011522360.1 |
XM_011524059.2 | 2654 | Missense Mutation | CAG,CGG | Q69R | XP_011522361.1 |
XM_017025290.1 | 2654 | Missense Mutation | CAG,CGG | Q69R | XP_016880779.1 |