Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001318192.1 | 2368 | Missense Mutation | AGC,TGC | S554C | NP_001305121.1 |
NM_012450.3 | 2368 | Missense Mutation | AGC,TGC | S553C | NP_036582.2 |
XM_011516024.2 | 2368 | Intron | XP_011514326.1 | ||
XM_017011962.1 | 2368 | Missense Mutation | AGC,TGC | S502C | XP_016867451.1 |
XM_017011963.1 | 2368 | Intron | XP_016867452.1 |