Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001624.3 | 5415 | Missense Mutation | TCC,TGC | S1643C | NP_001615.2 |
XM_005266839.3 | 5415 | Missense Mutation | TCC,TGC | S2051C | XP_005266896.1 |
XM_017010333.1 | 5415 | UTR 3 | XP_016865822.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001318746.1 | 5415 | Intron | NP_001305675.1 | ||
NM_032730.5 | 5415 | Intron | NP_116119.2 | ||
XM_011536192.2 | 5415 | Intron | XP_011534494.1 | ||
XM_017011375.1 | 5415 | Intron | XP_016866864.1 | ||
XM_017011376.1 | 5415 | Intron | XP_016866865.1 |