Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001308220.1 | 2873 | Missense Mutation | CTC,TTC | L854F | NP_001295149.2 |
NM_033266.3 | 2873 | Missense Mutation | CTC,TTC | L906F | NP_150296.4 |
XM_011545708.1 | 2873 | Missense Mutation | CTC,TTC | L762F | XP_011544010.1 |
XM_011545709.1 | 2873 | Missense Mutation | CTC,TTC | L762F | XP_011544011.1 |
XM_011545711.2 | 2873 | Intron | XP_011544013.1 | ||
XM_011545712.2 | 2873 | Intron | XP_011544014.1 | ||
XM_011545713.1 | 2873 | Intron | XP_011544015.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_005030.5 | 2873 | Intron | NP_005021.2 |