Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001301054.1 | 664 | Missense Mutation | ACG,ATG | T184M | NP_001287983.1 |
NM_001301057.1 | 664 | Intron | NP_001287986.1 | ||
NM_024028.3 | 664 | Missense Mutation | ACG,ATG | T201M | NP_076933.3 |
XM_011537680.1 | 664 | Missense Mutation | ACG,ATG | T83M | XP_011535982.1 |
XM_011537681.1 | 664 | Missense Mutation | ACG,ATG | T83M | XP_011535983.1 |
XM_011537682.2 | 664 | Intron | XP_011535984.1 |