Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001286526.1 | 1212 | Missense Mutation | CTC,TTC | L200F | NP_001273455.1 |
NM_004765.3 | 1212 | Intron | NP_004756.2 | ||
XM_011545980.2 | 1212 | Intron | XP_011544282.1 | ||
XM_017023885.1 | 1212 | Intron | XP_016879374.1 | ||
XM_017023886.1 | 1212 | UTR 3 | XP_016879375.1 | ||
XM_017023887.1 | 1212 | Intron | XP_016879376.1 | ||
XM_017023888.1 | 1212 | Intron | XP_016879377.1 |