Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001243738.1 | 2684 | Missense Mutation | CAG,CGG | Q692R | NP_001230667.1 |
NM_004761.4 | 2684 | Missense Mutation | CAG,CGG | Q774R | NP_004752.1 |
XM_011514781.1 | 2684 | Missense Mutation | CAG,CGG | Q667R | XP_011513083.1 |
XM_011514785.2 | 2684 | Intron | XP_011513087.1 |