Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_017855.3 | 138 | Missense Mutation | CTT,TTT | L41F | NP_060325.3 |
XM_005265698.3 | 138 | Missense Mutation | CTT,TTT | L58F | XP_005265755.1 |
XM_006714245.3 | 138 | Missense Mutation | CTT,TTT | L58F | XP_006714308.1 |
XM_017008331.1 | 138 | Missense Mutation | CTT,TTT | L27F | XP_016863820.1 |