Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_002551.3 | 913 | Missense Mutation | CCT,GCT | P292A | NP_002542.3 |
XM_017024697.1 | 913 | Missense Mutation | CCT,GCT | P294A | XP_016880186.1 |
XM_017024698.1 | 913 | Missense Mutation | CCT,GCT | P294A | XP_016880187.1 |