Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000438.5 | 1816 | Intron | NP_000429.2 | ||
NM_001127366.2 | 1816 | Missense Mutation | CTC,TTC | L478F | NP_001120838.1 |
NM_013942.4 | 1816 | Intron | NP_039230.1 | ||
NM_181457.3 | 1816 | Intron | NP_852122.1 | ||
NM_181458.3 | 1816 | Missense Mutation | CTC,TTC | L479F | NP_852123.1 |
NM_181459.3 | 1816 | Missense Mutation | CTC,TTC | L479F | NP_852124.1 |
NM_181460.3 | 1816 | Silent Mutation | ATC,ATT | I396I | NP_852125.1 |
NM_181461.3 | 1816 | Silent Mutation | ATC,ATT | I396I | NP_852126.1 |