Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001142364.1 | 942 | Missense Mutation | CCA,CTA | P262L | NP_001135836.1 |
NM_013338.4 | 942 | Missense Mutation | CCA,CTA | P292L | NP_037470.1 |
XM_017020552.1 | 942 | Missense Mutation | CCA,CTA | P229L | XP_016876041.1 |