Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006851.2 | 844 | Missense Mutation | CGT,TGT | R216C | NP_006842.2 |
XM_011537775.2 | 844 | Silent Mutation | AAC,AAT | N239N | XP_011536077.1 |
XM_017018721.1 | 844 | Silent Mutation | AAC,AAT | N98N | XP_016874210.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_007043.6 | 844 | UTR 3 | NP_008974.5 |