Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001014987.1 | 380 | Missense Mutation | ATG,GTG | M10V | NP_001014987.1 |
NM_001014988.1 | 380 | Missense Mutation | ATG,GTG | M10V | NP_001014988.1 |
NM_001014989.1 | 380 | Missense Mutation | ATG,GTG | M46V | NP_001014989.2 |
NM_014387.3 | 380 | Missense Mutation | ATG,GTG | M10V | NP_055202.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001142448.1 | 380 | Intron | NP_001135920.1 | ||
NM_001142449.1 | 380 | Intron | NP_001135921.1 | ||
NM_001142450.1 | 380 | Intron | NP_001135922.1 | ||
NM_001142451.1 | 380 | Intron | NP_001135923.1 | ||
NM_032038.2 | 380 | Intron | NP_114427.1 | ||
XM_006721096.3 | 380 | Intron | XP_006721159.1 | ||
XM_017023757.1 | 380 | Intron | XP_016879246.1 | ||
XM_017023758.1 | 380 | Intron | XP_016879247.1 | ||
XM_017023759.1 | 380 | Intron | XP_016879248.1 |