Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_181536.1 | 4753 | Missense Mutation | AGC,TGC | S1585C | NP_853514.1 |
XM_017023201.1 | 4753 | Intron | XP_016878690.1 | ||
XM_017023202.1 | 4753 | Intron | XP_016878691.1 | ||
XM_017023203.1 | 4753 | Intron | XP_016878692.1 | ||
XM_017023204.1 | 4753 | Intron | XP_016878693.1 |