Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001144072.1 | 206 | Intron | NP_001137544.1 | ||
NM_177967.3 | 206 | Missense Mutation | GCT,GTT | A47V | NP_808882.1 |
XM_006719948.3 | 206 | UTR 5 | XP_006720011.1 | ||
XM_011521082.2 | 206 | Intron | XP_011519384.1 | ||
XM_011521083.2 | 206 | Missense Mutation | GCT,GTT | A30V | XP_011519385.1 |
XM_011521084.2 | 206 | Intron | XP_011519386.1 | ||
XM_017020553.1 | 206 | Intron | XP_016876042.1 |