ENST00000644719.2:c.602C>A
MANE Select
|
ENSP00000496625.1:p.Thr201Asn
|
|
ENST00000418967.6:c.602C>A
|
ENSP00000408860.2:p.Thr201Asn
|
|
ENST00000435122.3:c.512C>A
|
ENSP00000415043.2:p.Thr171Asn
|
|
ENST00000462278.1:n.190C>A
|
|
|
ENST00000464325.5:n.523C>A
|
|
|
ENST00000466779.5:c.*294C>A
|
ENSP00000417321.1:n.*294C>A
|
|
ENST00000466879.5:n.653C>A
|
|
|
ENST00000469053.5:c.*294C>A
|
ENSP00000418104.1:n.*294C>A
|
|
ENST00000471671.4:c.563C>A
|
ENSP00000418561.1:p.Thr188Asn
|
|
ENST00000479074.5:n.660C>A
|
|
|
ENST00000479730.5:n.718C>A
|
|
|
ENST00000483041.5:n.771C>A
|
|
|
ENST00000486063.5:n.782C>A
|
|
|
NM_000500.7:c.602C>A
|
NP_000491.4:p.Thr201Asn
|
|
NM_001128590.3:c.512C>A
|
NP_001122062.3:p.Thr171Asn
|
|
XM_011514314.1:c.197C>A
|
XP_011512616.1:p.Thr66Asn
|
|
NM_000500.9:c.602C>A
MANE Select
|
NP_000491.4:p.Thr201Asn
|
|
NM_001368143.1:c.197C>A
|
NP_001355072.1:p.Thr66Asn
|
|
NM_001368144.1:c.197C>A
|
NP_001355073.1:p.Thr66Asn
|
|
NM_001128590.4:c.512C>A
|
NP_001122062.3:p.Thr171Asn
|
|
NM_001368143.2:c.197C>A
|
NP_001355072.1:p.Thr66Asn
|
|
NM_001368144.2:c.197C>A
|
NP_001355073.1:p.Thr66Asn
|
|