Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_022761.2 | 636 | Missense Mutation | AAA,ACA | K100T | NP_073598.1 |
XM_011542957.2 | 636 | Missense Mutation | AAA,ACA | K116T | XP_011541259.1 |
XM_011542958.2 | 636 | Intron | XP_011541260.1 | ||
XM_017018129.1 | 636 | Intron | XP_016873618.1 |