Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006950.3 | 422 | Intron | NP_008881.2 | ||
NM_133499.2 | 422 | Intron | NP_598006.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_003254.2 | 422 | Silent Mutation | GTC,GTG | V92V | NP_003245.1 |
XM_017029766.1 | 422 | Missense Mutation | TCT,TGT | S16C | XP_016885255.1 |