Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001023560.3 | 339 | Missense Mutation | CAG,CGG | Q73R | NP_001018854.2 |
NM_001111039.2 | 339 | Missense Mutation | CAG,CGG | Q73R | NP_001104509.1 |
NM_001287421.1 | 339 | Intron | NP_001274350.1 | ||
NM_001287422.1 | 339 | Intron | NP_001274351.1 | ||
NM_152736.5 | 339 | Intron | NP_689949.3 | ||
XM_011514862.2 | 339 | Missense Mutation | CAG,CGG | Q73R | XP_011513164.1 |
XM_011514864.1 | 339 | Missense Mutation | CAG,CGG | Q44R | XP_011513166.1 |
XM_011514866.1 | 339 | Intron | XP_011513168.1 | ||
XM_011514867.1 | 339 | UTR 5 | XP_011513169.1 | ||
XM_011514869.1 | 339 | UTR 5 | XP_011513171.1 | ||
XM_017011264.1 | 339 | Missense Mutation | CAG,CGG | Q73R | XP_016866753.1 |
XM_017011265.1 | 339 | UTR 5 | XP_016866754.1 |