Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_032827.6 | 1045 | Missense Mutation | CCG,CTG | P214L | NP_116216.2 |
XM_006712122.3 | 1045 | Missense Mutation | CCG,CTG | P214L | XP_006712185.1 |
XM_011533139.1 | 1045 | Missense Mutation | CCG,CTG | P214L | XP_011531441.1 |