Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001243877.1 | 1069 | Missense Mutation | CCT,GCT | P277A | NP_001230806.1 |
NM_001243885.1 | 1069 | Missense Mutation | CCT,GCT | P138A | NP_001230814.1 |
NM_005749.3 | 1069 | Missense Mutation | CCT,GCT | P277A | NP_005740.1 |