Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001136537.1 | 483 | Missense Mutation | TTC,TTG | F48L | NP_001130009.1 |
XM_006710386.3 | 483 | Missense Mutation | TTC,TTG | F48L | XP_006710449.1 |
XM_011540803.2 | 483 | Missense Mutation | TTC,TTG | F48L | XP_011539105.1 |
XM_011540805.2 | 483 | Missense Mutation | TTC,TTG | F48L | XP_011539107.1 |
XM_017000447.1 | 483 | Missense Mutation | TTC,TTG | F48L | XP_016855936.1 |
XM_017000448.1 | 483 | Missense Mutation | TTC,TTG | F48L | XP_016855937.1 |
XM_017000449.1 | 483 | Missense Mutation | TTC,TTG | F48L | XP_016855938.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001013632.3 | 483 | Intron | NP_001013654.1 |