Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000499.4 | 1620 | Missense Mutation | CCG,CTG | P474L | NP_000490.1 |
NM_001319216.1 | 1620 | Missense Mutation | CCG,CTG | P445L | NP_001306145.1 |
NM_001319217.1 | 1620 | Missense Mutation | CCG,CTG | P474L | NP_001306146.1 |
XM_017021953.1 | 1620 | Missense Mutation | CCG,CTG | P446L | XP_016877442.1 |