Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_004851.2 | 1674 | Missense Mutation | ACG,ATG | T380M | NP_004842.1 |
XM_011527540.1 | 1674 | Missense Mutation | ACG,ATG | T380M | XP_011525842.1 |
XM_017027512.1 | 1674 | Missense Mutation | ACG,ATG | T371M | XP_016883001.1 |