Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_021833.4 | 899 | Missense Mutation | CTC,TTC | L275F | NP_068605.1 |
XM_005263206.3 | 899 | Missense Mutation | CTC,TTC | L274F | XP_005263263.1 |
XM_011532228.2 | 899 | Intron | XP_011530530.1 |