Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_005282.2 | 2609 | Missense Mutation | CCG,CTG | P359L | NP_005273.1 |
XM_017026607.1 | 2609 | Missense Mutation | CCG,CTG | P359L | XP_016882096.1 |
XM_017026608.1 | 2609 | Missense Mutation | CCG,CTG | P359L | XP_016882097.1 |