Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001320546.1 | 383 | Missense Mutation | CCT,CTT | P117L | NP_001307475.1 |
NM_001320547.1 | 383 | Missense Mutation | CCT,CTT | P92L | NP_001307476.1 |
NM_018031.4 | 383 | Missense Mutation | CCT,CTT | P173L | NP_060501.3 |