Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006051.3 | 1647 | Missense Mutation | CGC,TGC | R439C | NP_006042.3 |
NM_133172.2 | 1647 | Missense Mutation | CGC,TGC | R437C | NP_573418.2 |
NM_133173.2 | 1647 | Missense Mutation | CGC,TGC | R432C | NP_573419.2 |
NM_133174.2 | 1647 | Missense Mutation | CGC,TGC | R430C | NP_573420.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001035235.3 | 1647 | Intron | NP_001030312.2 | ||
NM_001253764.1 | 1647 | Intron | NP_001240693.1 |