Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001291726.1 | 646 | Missense Mutation | CAG,CGG | Q197R | NP_001278655.1 |
NM_001291728.1 | 646 | Missense Mutation | CAG,CGG | Q227R | NP_001278657.1 |
NM_001291730.1 | 646 | Intron | NP_001278659.1 | ||
NM_001291732.1 | 646 | Intron | NP_001278661.1 | ||
NM_001291733.1 | 646 | Intron | NP_001278662.1 | ||
NM_033419.4 | 646 | Missense Mutation | CAG,CGG | Q248R | NP_219487.3 |
XM_011525480.2 | 646 | Intron | XP_011523782.1 | ||
XM_011525481.2 | 646 | Missense Mutation | CAG,CGG | Q133R | XP_011523783.1 |