Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000263.3 | 165 | Missense Mutation | TTA,TTC | L48F | NP_000254.2 |
XM_006721920.2 | 165 | Intron | XP_006721983.1 | ||
XM_011524840.1 | 165 | Intron | XP_011523142.1 | ||
XM_017024686.1 | 165 | UTR 5 | XP_016880175.1 | ||
XM_017024687.1 | 165 | Intron | XP_016880176.1 |