Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001177716.1 | 292 | Missense Mutation | CCT,CTT | P75L | NP_001171187.1 |
NM_001177718.1 | 292 | Missense Mutation | CCT,CTT | P75L | NP_001171189.1 |
NM_003597.4 | 292 | Missense Mutation | CCT,CTT | P92L | NP_003588.1 |