Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001323538.1 | 232 | Intron | NP_001310467.1 | ||
NM_001761.2 | 232 | Intron | NP_001752.2 | ||
XM_017023822.1 | 232 | Missense Mutation | CCA,CTA | P76L | XP_016879311.1 |
XM_017023823.1 | 232 | Missense Mutation | CCA,CTA | P76L | XP_016879312.1 |