Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_017708.3 | 913 | Missense Mutation | ACG,ATG | T283M | NP_060178.2 |
XM_005259019.1 | 913 | Missense Mutation | ACG,ATG | T283M | XP_005259076.1 |
XM_011527049.2 | 913 | Intron | XP_011525351.1 |