Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001243211.1 | 666 | Missense Mutation | ACG,ATG | T145M | NP_001230140.1 |
NM_001562.3 | 666 | Missense Mutation | ACG,ATG | T149M | NP_001553.1 |
XM_011542805.1 | 666 | Missense Mutation | ACG,ATG | T145M | XP_011541107.1 |
XM_011542806.2 | 666 | Missense Mutation | ACG,ATG | T149M | XP_011541108.1 |