Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001290104.1 | 2549 | Missense Mutation | CCA,CTA | P689L | NP_001277033.1 |
NM_003460.2 | 2549 | Missense Mutation | CCA,CTA | P698L | NP_003451.1 |
XM_011545942.2 | 2549 | Missense Mutation | XP_011544244.1 |