Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001297701.1 | 579 | Missense Mutation | CCT,GCT | P148A | NP_001284630.1 |
NM_032878.3 | 579 | Missense Mutation | CCT,GCT | P176A | NP_116267.3 |
NM_198867.1 | 579 | UTR 3 | NP_942567.1 | ||
XM_005259357.4 | 579 | Missense Mutation | CCT,GCT | P148A | XP_005259414.1 |