Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001282382.1 | 716 | Missense Mutation | CCT,TCT | P105S | NP_001269311.1 |
NM_001282383.1 | 716 | Missense Mutation | CCT,TCT | P105S | NP_001269312.1 |
NM_004219.3 | 716 | Missense Mutation | CCT,TCT | P105S | NP_004210.1 |