Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001301076.1 | 329 | Intron | NP_001288005.1 | ||
NM_001301078.1 | 329 | Missense Mutation | AGC,ATC | S55I | NP_001288007.1 |
NM_001301081.1 | 329 | Intron | NP_001288010.1 | ||
NM_004069.4 | 329 | Intron | NP_004060.2 | ||
NM_021575.3 | 329 | Intron | NP_067586.1 | ||
XM_011526423.2 | 329 | Missense Mutation | AGC,ATC | S71I | XP_011524725.1 |
XM_011526424.2 | 329 | Missense Mutation | AGC,ATC | S57I | XP_011524726.1 |