Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001013743.2 | 1772 | Intron | NP_001013765.2 | ||
XM_006718832.3 | 1772 | Intron | XP_006718895.1 | ||
XM_011542802.2 | 1772 | Intron | XP_011541104.1 | ||
XM_017017653.1 | 1772 | Missense Mutation | CCC,CTC | P145L | XP_016873142.1 |