Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001142798.2 | 207 | Missense Mutation | CCG,CTG | P29L | NP_001136270.1 |
NM_001142799.2 | 207 | Missense Mutation | CCG,CTG | P29L | NP_001136271.1 |
NM_174893.3 | 207 | Missense Mutation | CCG,CTG | P29L | NP_777553.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001004333.4 | 207 | Intron | NP_001004333.2 |