Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001031666.1 | 129 | Intron | NP_001026836.1 | ||
NM_001031809.1 | 129 | Missense Mutation | ATG,GTG | M1V | NP_001026979.1 |
NM_006138.4 | 129 | Missense Mutation | ATG,GTG | M1V | NP_006129.4 |
XM_011545363.2 | 129 | Intron | XP_011543665.1 |