ENST00000489304.6:c.932A>G
|
ENSP00000512096.1:n.932A>G
|
|
ENST00000695675.1:n.2725A>G
|
|
|
ENST00000372285.8:c.*15A>G
MANE Select
|
ENSP00000361359.3:n.*15A>G
|
|
ENST00000372276.7:c.*175A>G
|
ENSP00000361350.3:n.*175A>G
|
|
ENST00000372285.7:c.*15A>G
|
ENSP00000361359.3:n.*15A>G
|
|
ENST00000466205.5:c.751A>G
|
|
|
ENST00000489304.5:n.925A>G
|
|
|
ENST00000620709.4:c.*396A>G
|
ENSP00000484074.1:n.*396A>G
|
|
NM_001250.5:c.*15A>G
|
NP_001241.1:n.*15A>G
|
|
NM_001302753.1:c.*175A>G
|
NP_001289682.1:n.*175A>G
|
|
NM_152854.3:c.*175A>G
|
NP_690593.1:n.*175A>G
|
|
NR_126502.1:n.942A>G
|
|
|
XM_005260617.2:c.*15A>G
|
XP_005260674.1:n.*15A>G
|
|
XM_005260619.2:c.*15A>G
|
XP_005260676.1:n.*15A>G
|
|
NM_001322421.1:c.*15A>G
|
NP_001309350.1:n.*15A>G
|
|
NM_001322422.1:c.*15A>G
|
NP_001309351.1:n.*15A>G
|
|
NM_001362758.1:c.*175A>G
|
NP_001349687.1:n.*175A>G
|
|
NR_136327.1:n.845A>G
|
|
|
XM_005260619.3:c.*15A>G
|
XP_005260676.1:n.*15A>G
|
|
XM_017028135.1:c.884A>G
|
XP_016883624.1:p.Gln295Arg
|
|
XM_017028136.1:c.782A>G
|
XP_016883625.1:p.Gln261Arg
|
|
NM_001250.6:c.*15A>G
MANE Select
|
NP_001241.1:n.*15A>G
|
|
NM_001302753.2:c.*175A>G
|
NP_001289682.1:n.*175A>G
|
|
NM_001322421.2:c.*15A>G
|
NP_001309350.1:n.*15A>G
|
|
NM_001322422.2:c.*15A>G
|
NP_001309351.1:n.*15A>G
|
|
NM_001362758.2:c.*175A>G
|
NP_001349687.1:n.*175A>G
|
|
NM_152854.4:c.*175A>G
|
NP_690593.1:n.*175A>G
|
|
NR_126502.2:n.882A>G
|
|
|
NR_136327.2:n.785A>G
|
|
|