Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_003215.2 | 2976 | Missense Mutation | ACG,ATG | T560M | NP_003206.2 |
XM_011513737.2 | 2976 | Missense Mutation | ACG,ATG | T524M | XP_011512039.1 |
XM_011513741.1 | 2976 | Intron | XP_011512043.1 | ||
XM_017008569.1 | 2976 | Missense Mutation | ACG,ATG | T444M | XP_016864058.1 |