Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001136215.1 | 796 | Missense Mutation | CCT,CTT | P5L | NP_001129687.1 |
NM_057090.2 | 796 | Missense Mutation | CCT,CTT | P5L | NP_476431.2 |
NM_057091.2 | 796 | Missense Mutation | CCT,CTT | P5L | NP_476432.2 |