Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_024308.3 | 690 | Missense Mutation | CCC,CTC | P159L | NP_077284.2 |
XM_005257658.2 | 690 | Missense Mutation | CCC,CTC | P159L | XP_005257715.1 |
XM_011525233.2 | 690 | Missense Mutation | CCC,CTC | P89L | XP_011523535.1 |