Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001313892.1 | 1234 | Missense Mutation | CCT,CTT | P98L | NP_001300821.1 |
NM_001313893.1 | 1234 | Missense Mutation | CCT,CTT | P98L | NP_001300822.1 |
NM_002128.5 | 1234 | Missense Mutation | CCT,CTT | P98L | NP_002119.1 |