Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001307923.1 | 292 | Missense Mutation | CTC,TTC | L42F | NP_001294852.1 |
NM_012397.3 | 292 | Missense Mutation | CTC,TTC | L42F | NP_036529.1 |
XM_005266707.3 | 292 | UTR 5 | XP_005266764.1 | ||
XM_011526029.2 | 292 | Missense Mutation | CTC,TTC | L42F | XP_011524331.1 |