Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_004951.4 | 1138 | Missense Mutation | ATG,GTG | M322V | NP_004942.1 |
XM_017020405.1 | 1138 | Missense Mutation | ATG,GTG | M322V | XP_016875894.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001144072.1 | 1138 | Intron | NP_001137544.1 | ||
NM_177967.3 | 1138 | Intron | NP_808882.1 | ||
XM_006719948.3 | 1138 | Intron | XP_006720011.1 | ||
XM_011521082.2 | 1138 | Intron | XP_011519384.1 | ||
XM_011521083.2 | 1138 | Intron | XP_011519385.1 | ||
XM_011521084.2 | 1138 | Intron | XP_011519386.1 | ||
XM_017020553.1 | 1138 | Intron | XP_016876042.1 |