Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001161342.2 | 406 | Missense Mutation | ATG,GTG | M68V | NP_001154814.1 |
NM_173490.7 | 406 | Missense Mutation | ATG,GTG | M68V | NP_775761.4 |
XM_011543156.1 | 406 | Missense Mutation | ATG,GTG | M68V | XP_011541458.1 |