Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000884.2 | 1731 | Missense Mutation | TCT,TGT | S485C | NP_000875.2 |
XM_006713128.3 | 1731 | Missense Mutation | TCT,TGT | S579C | XP_006713191.1 |
XM_017006349.1 | 1731 | Missense Mutation | TCT,TGT | S554C | XP_016861838.1 |
XM_017006350.1 | 1731 | Missense Mutation | TCT,TGT | S530C | XP_016861839.1 |