|
ENST00000682775.1:c.2185+17535A>G
|
ENSP00000508399.1:n.2185+17535A>G
|
|
|
ENST00000682944.1:c.7653A>G
|
ENSP00000507173.1:p.Glu2551=
|
|
|
ENST00000683210.1:c.2185+17535A>G
|
ENSP00000506739.1:n.2185+17535A>G
|
|
|
ENST00000683270.1:c.6445+1172A>G
|
ENSP00000507624.1:n.6445+1172A>G
|
|
|
ENST00000683367.1:c.2177-6766A>G
|
ENSP00000507780.1:n.2177-6766A>G
|
|
|
ENST00000683489.1:c.2291+5335A>G
|
ENSP00000508403.1:n.2291+5335A>G
|
|
|
ENST00000683680.1:c.2318+5335A>G
|
ENSP00000507223.1:n.2318+5335A>G
|
|
|
ENST00000684163.1:c.2204-6766A>G
|
ENSP00000508262.1:n.2204-6766A>G
|
|
|
ENST00000684196.1:n.4543-6766A>G
|
|
|
|
ENST00000684325.1:c.2186-14576A>G
|
ENSP00000508121.1:n.2186-14576A>G
|
|
|
ENST00000684385.1:c.2221-6766A>G
|
ENSP00000507855.1:n.2221-6766A>G
|
|
|
ENST00000684497.1:c.2186-13606A>G
|
ENSP00000507057.1:n.2186-13606A>G
|
|
|
ENST00000382292.9:c.7626A>G
MANE Select
|
ENSP00000371729.3:p.Glu2542=
|
|
|
ENST00000423156.2:c.2186-6766A>G
|
ENSP00000390925.2:n.2186-6766A>G
|
|
|
ENST00000455470.6:c.2431+5195A>G
|
ENSP00000406565.2:n.2431+5195A>G
|
|
|
ENST00000382292.7:c.7626A>G
|
ENSP00000371729.3:p.Glu2542=
|
|
|
ENST00000382298.7:c.7626A>G
|
ENSP00000371735.3:p.Glu2542=
|
|
|
ENST00000402364.1:c.5376A>G
|
ENSP00000385844.1:p.Glu1792=
|
|
|
ENST00000423156.1:c.1058-6766A>G
|
ENSP00000390925.1:n.1058-6766A>G
|
|
|
ENST00000455470.5:c.2129+5195A>G
|
|
|
|
NM_001278055.1:c.7185A>G
|
NP_001264984.1:p.Glu2395=
|
|
|
NM_014363.5:c.7626A>G
|
NP_055178.3:p.Glu2542=
|
|
|
XM_005266338.1:c.7653A>G
|
XP_005266395.1:p.Glu2551=
|
|
|
XM_011535038.1:c.7677A>G
|
XP_011533340.1:p.Glu2559=
|
|
|
XM_011535039.1:c.7644A>G
|
XP_011533341.1:p.Glu2548=
|
|
|
XM_005266338.2:c.7653A>G
|
XP_005266395.1:p.Glu2551=
|
|
|
XM_011535039.2:c.7644A>G
|
XP_011533341.1:p.Glu2548=
|
|
|
XM_017020539.1:c.7617A>G
|
XP_016876028.1:p.Glu2539=
|
|
|
XM_024449337.1:c.7653A>G
|
XP_024305105.1:p.Glu2551=
|
|
|
NM_014363.6:c.7626A>G
MANE Select
|
NP_055178.3:p.Glu2542=
|
|
|
NM_001278055.2:c.7185A>G
|
NP_001264984.1:p.Glu2395=
|
|
