Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001142448.1 | 432 | Missense Mutation | AGG,GGG | R19G | NP_001135920.1 |
NM_001142449.1 | 432 | Missense Mutation | AGG,GGG | R19G | NP_001135921.1 |
NM_001142450.1 | 432 | UTR 5 | NP_001135922.1 | ||
NM_001142451.1 | 432 | Missense Mutation | AGG,GGG | R19G | NP_001135923.1 |
NM_032038.2 | 432 | Missense Mutation | AGG,GGG | R19G | NP_114427.1 |
XM_006721096.3 | 432 | Missense Mutation | AGG,GGG | R64G | XP_006721159.1 |
XM_017023757.1 | 432 | Missense Mutation | AGG,GGG | R64G | XP_016879246.1 |
XM_017023758.1 | 432 | Missense Mutation | AGG,GGG | R64G | XP_016879247.1 |
XM_017023759.1 | 432 | Missense Mutation | AGG,GGG | R64G | XP_016879248.1 |