Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_139286.3 | 823 | Intron | NP_644815.1 | ||
XM_017014573.1 | 823 | Intron | XP_016870062.1 | ||
XM_017014574.1 | 823 | Missense Mutation | CCA,CTA | P11L | XP_016870063.1 |
XM_017014575.1 | 823 | Intron | XP_016870064.1 |