Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006051.3 | 1798 | Missense Mutation | CCG,CTG | P489L | NP_006042.3 |
NM_133172.2 | 1798 | Missense Mutation | CCG,CTG | P487L | NP_573418.2 |
NM_133173.2 | 1798 | Missense Mutation | CCG,CTG | P482L | NP_573419.2 |
NM_133174.2 | 1798 | Missense Mutation | CCG,CTG | P480L | NP_573420.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001035235.3 | 1798 | Intron | NP_001030312.2 | ||
NM_001253764.1 | 1798 | Intron | NP_001240693.1 |