ENST00000321854.13:c.*1C>G
MANE Select
|
ENSP00000314440.8:n.*1C>G
|
|
ENST00000321854.12:c.*1C>G
|
ENSP00000314440.8:n.*1C>G
|
|
ENST00000398322.7:c.*1C>G
|
ENSP00000381367.2:n.*1C>G
|
|
ENST00000431281.5:c.957C>G
|
ENSP00000405969.1:p.Asp319Glu
|
|
ENST00000585553.5:n.1637C>G
|
|
|
ENST00000586346.5:c.957C>G
|
ENSP00000465484.1:p.Asp319Glu
|
|
ENST00000591859.5:c.957C>G
|
ENSP00000465610.1:p.Asp319Glu
|
|
ENST00000592162.5:c.779C>G
|
ENSP00000466305.1:p.Thr260Ser
|
|
NM_001135704.1:c.957C>G
|
NP_001129176.1:p.Asp319Glu
|
|
NM_001135705.1:c.*1C>G
|
NP_001129177.1:n.*1C>G
|
|
NM_001135706.1:c.957C>G
|
NP_001129178.1:p.Asp319Glu
|
|
NM_024722.2:c.*1C>G
|
NP_078998.1:n.*1C>G
|
|
XM_005257673.1:c.960C>G
|
XP_005257730.1:p.Asp320Glu
|
|
XM_005257674.1:c.960C>G
|
XP_005257731.1:p.Asp320Glu
|
|
XM_005257677.1:c.957C>G
|
XP_005257734.1:p.Asp319Glu
|
|
XM_006722085.1:c.*1C>G
|
XP_006722148.1:n.*1C>G
|
|
XM_006722088.1:c.*1C>G
|
XP_006722151.1:n.*1C>G
|
|
XM_006722089.1:c.782C>G
|
XP_006722152.1:p.Thr261Ser
|
|
XM_006722090.1:c.779C>G
|
XP_006722153.1:p.Thr260Ser
|
|
XM_011525255.1:c.960C>G
|
XP_011523557.1:p.Asp320Glu
|
|
XM_011525256.1:c.960C>G
|
XP_011523558.1:p.Asp320Glu
|
|
XM_011525257.1:c.*1C>G
|
XP_011523559.1:n.*1C>G
|
|
NM_001135705.2:c.*1C>G
|
NP_001129177.1:n.*1C>G
|
|
NM_001135706.2:c.957C>G
|
NP_001129178.1:p.Asp319Glu
|
|
NM_001135707.2:c.*962C>G
|
NP_001129179.1:n.*962C>G
|
|
NM_001321352.1:c.957C>G
|
NP_001308281.1:p.Asp319Glu
|
|
NM_001321353.1:c.957C>G
|
NP_001308282.1:p.Asp319Glu
|
|
NM_024722.3:c.*1C>G
|
NP_078998.1:n.*1C>G
|
|
XM_006722085.2:c.*1C>G
|
XP_006722148.1:n.*1C>G
|
|
XM_017025084.1:c.978C>G
|
XP_016880573.1:p.Asp326Glu
|
|
XM_017025085.1:c.978C>G
|
XP_016880574.1:p.Asp326Glu
|
|
XM_017025086.1:c.978C>G
|
XP_016880575.1:p.Asp326Glu
|
|
XM_017025087.1:c.960C>G
|
XP_016880576.1:p.Asp320Glu
|
|
XM_017025088.1:c.957C>G
|
XP_016880577.1:p.Asp319Glu
|
|
XM_017025089.2:c.*792C>G
|
XP_016880578.1:n.*792C>G
|
|
XM_017025090.1:c.*1C>G
|
XP_016880579.1:n.*1C>G
|
|
XM_017025091.1:c.*1C>G
|
XP_016880580.1:n.*1C>G
|
|
XM_017025092.2:c.*1C>G
|
XP_016880581.1:n.*1C>G
|
|
XM_017025094.1:c.*962C>G
|
XP_016880583.1:n.*962C>G
|
|
XM_017025095.1:c.*1C>G
|
XP_016880584.1:n.*1C>G
|
|
XM_017025096.1:c.800C>G
|
XP_016880585.1:p.Thr267Ser
|
|
XM_017025097.1:c.*1C>G
|
XP_016880586.1:n.*1C>G
|
|
XM_017025098.1:c.*1C>G
|
XP_016880587.1:n.*1C>G
|
|
XM_017025099.1:c.779C>G
|
XP_016880588.1:p.Thr260Ser
|
|
XM_024450949.1:c.*792C>G
|
XP_024306717.1:n.*792C>G
|
|
NM_001135705.3:c.*1C>G
MANE Select
|
NP_001129177.1:n.*1C>G
|
|
NM_001135706.3:c.957C>G
|
NP_001129178.1:p.Asp319Glu
|
|
NM_001135707.3:c.*962C>G
|
NP_001129179.1:n.*962C>G
|
|
NM_001321352.2:c.957C>G
|
NP_001308281.1:p.Asp319Glu
|
|
NM_001321353.2:c.957C>G
|
NP_001308282.1:p.Asp319Glu
|
|
NM_024722.4:c.*1C>G
|
NP_078998.1:n.*1C>G
|
|
NM_001378111.1:c.*962C>G
|
NP_001365040.1:n.*962C>G
|
|
NM_001378112.1:c.*962C>G
|
NP_001365041.1:n.*962C>G
|
|