Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001161619.1 | 1814 | Missense Mutation | CGC,TGC | R331C | NP_001155091.1 |
NM_020175.2 | 1814 | Missense Mutation | CGC,TGC | R573C | NP_064560.2 |
XM_017027020.1 | 1814 | Missense Mutation | CGC,TGC | R559C | XP_016882509.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001134316.1 | 1814 | Intron | NP_001127788.1 |