Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_152643.6 | 404 | Missense Mutation | CCT,CTT | P11L | NP_689856.6 |
XM_017016858.1 | 404 | Missense Mutation | CCT,CTT | P11L | XP_016872347.1 |
XM_017016859.1 | 404 | Missense Mutation | CCT,CTT | P11L | XP_016872348.1 |