Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001005291.2 | 3537 | Missense Mutation | CCG,GCG | P1145A | NP_001005291.1 |
NM_001321096.2 | 3537 | Missense Mutation | CCG,GCG | P1091A | NP_001308025.1 |
NM_004176.4 | 3537 | Missense Mutation | CCG,GCG | P1115A | NP_004167.3 |
XM_005256772.4 | 3537 | Missense Mutation | CCG,GCG | P1113A | XP_005256829.1 |
XM_017024970.1 | 3537 | Missense Mutation | CCG,GCG | P734A | XP_016880459.1 |
XM_017024971.1 | 3537 | Missense Mutation | CCG,GCG | P634A | XP_016880460.1 |