Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001271665.1 | 692 | Missense Mutation | AAG,CAG | K108Q | NP_001258594.1 |
NM_014886.4 | 692 | Missense Mutation | AAG,CAG | K108Q | NP_055701.1 |
XM_011543098.1 | 692 | Intron | XP_011541400.1 | ||
XM_017008952.1 | 692 | Intron | XP_016864441.1 | ||
XM_017008953.1 | 692 | Intron | XP_016864442.1 |