Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001271830.1 | 214 | Missense Mutation | ATG,GTG | M53V | NP_001258759.1 |
NM_174895.2 | 214 | Missense Mutation | ATG,GTG | M69V | NP_777555.1 |
XM_006722639.2 | 214 | Missense Mutation | ATG,GTG | M32V | XP_006722702.1 |
XM_017026249.1 | 214 | Missense Mutation | ATG,GTG | M185V | XP_016881738.1 |
XM_017026250.1 | 214 | Missense Mutation | ATG,GTG | M185V | XP_016881739.1 |
XM_017026251.1 | 214 | Missense Mutation | ATG,GTG | M69V | XP_016881740.1 |
XM_017026252.1 | 214 | Missense Mutation | ATG,GTG | M32V | XP_016881741.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001171155.1 | 214 | Intron | NP_001164626.1 |