Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001308007.1 | 717 | Missense Mutation | CCG,GCG | P11A | NP_001294936.1 |
NM_003797.4 | 717 | Missense Mutation | CCG,GCG | P11A | NP_003788.2 |
XM_005274373.2 | 717 | Missense Mutation | CCG,GCG | P11A | XP_005274430.1 |
XM_011545330.1 | 717 | Missense Mutation | CCG,GCG | P11A | XP_011543632.1 |
XM_011545331.1 | 717 | Missense Mutation | CCG,GCG | P11A | XP_011543633.1 |
XM_017018512.1 | 717 | Missense Mutation | CCG,GCG | P11A | XP_016874001.1 |
XM_017018513.1 | 717 | Missense Mutation | CCG,GCG | P11A | XP_016874002.1 |