Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_024578.2 | 91 | Missense Mutation | TCG,TTG | S16L | NP_078854.1 |
XM_005260079.2 | 91 | Intron | XP_005260136.1 | ||
XM_006722899.3 | 91 | Missense Mutation | TCG,TTG | S16L | XP_006722962.1 |
XM_017027306.1 | 91 | UTR 5 | XP_016882795.1 |