Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001166133.1 | 747 | Missense Mutation | TTG,TTT | L20F | NP_001159605.1 |
NM_025074.6 | 747 | Missense Mutation | TTG,TTT | L20F | NP_079350.5 |
XM_006714316.2 | 747 | Missense Mutation | TTG,TTT | L20F | XP_006714379.1 |