Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_003693.3 | 1391 | Missense Mutation | CCA,GCA | P800A | NP_003684.2 |
NM_145350.2 | 1391 | UTR 3 | NP_663325.1 | ||
XM_017025256.1 | 1391 | Missense Mutation | CCA,GCA | P389A | XP_016880745.1 |