Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001258040.2 | 1468 | Missense Mutation | ATG,GTG | M423V | NP_001244969.1 |
NM_001258041.2 | 1468 | Missense Mutation | ATG,GTG | M443V | NP_001244970.1 |
NM_001258042.2 | 1468 | Missense Mutation | ATG,GTG | M403V | NP_001244971.1 |
NM_001289092.1 | 1468 | Missense Mutation | ATG,GTG | M389V | NP_001276021.1 |
NM_001289093.1 | 1468 | Missense Mutation | ATG,GTG | M349V | NP_001276022.1 |
NM_001289094.1 | 1468 | Missense Mutation | ATG,GTG | M434V | NP_001276023.1 |
NM_002109.5 | 1468 | Missense Mutation | ATG,GTG | M463V | NP_002100.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_017706.4 | 1468 | Intron | NP_060176.2 | ||
XM_005268469.2 | 1468 | Intron | XP_005268526.1 | ||
XM_017009600.1 | 1468 | Intron | XP_016865089.1 |