Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_014008.4 | 1338 | Intron | NP_054727.1 | ||
XM_005272599.3 | 1338 | Intron | XP_005272656.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001114377.1 | 1338 | Missense Mutation | ACC,GCC | T349A | NP_001107849.1 |
NM_014009.3 | 1338 | Missense Mutation | ACC,GCC | T384A | NP_054728.2 |
XM_006724533.2 | 1338 | Missense Mutation | ACC,GCC | T407A | XP_006724596.2 |
XM_011543916.2 | 1338 | Missense Mutation | ACC,GCC | T517A | XP_011542218.1 |
XM_017029565.1 | 1338 | Missense Mutation | ACC,GCC | T469A | XP_016885054.1 |
XM_017029566.1 | 1338 | Missense Mutation | ACC,GCC | T457A | XP_016885055.1 |
XM_017029567.1 | 1338 | Missense Mutation | ACC,GCC | T426A | XP_016885056.1 |