ENST00000381129.8:c.952G>C
MANE Select
|
ENSP00000370521.3:p.Glu318Gln
|
|
ENST00000250087.9:c.763G>C
|
ENSP00000250087.5:p.Glu255Gln
|
|
ENST00000381128.2:c.*824G>C
|
ENSP00000370520.2:n.*824G>C
|
|
ENST00000381129.7:c.952G>C
|
ENSP00000370521.3:p.Glu318Gln
|
|
ENST00000570466.5:c.886G>C
|
ENSP00000461287.1:p.Glu296Gln
|
|
ENST00000570584.5:c.251+8256G>C
|
|
|
ENST00000574506.5:c.916G>C
|
ENSP00000458456.1:p.Glu306Gln
|
|
ENST00000575265.5:c.*923G>C
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ENSP00000459673.1:n.*923G>C
|
|
ENST00000576307.5:c.772G>C
|
ENSP00000459522.1:p.Glu258Gln
|
|
ENST00000576776.5:c.880G>C
|
ENSP00000460827.1:p.Glu294Gln
|
|
ENST00000621374.4:c.951G>C
|
ENSP00000481337.1:p.Arg317Ser
|
|
NM_001033054.2:c.763G>C
|
NP_001028226.1:p.Glu255Gln
|
|
NM_001033055.2:c.772G>C
|
NP_001028227.1:p.Glu258Gln
|
|
NM_001285399.2:c.916G>C
|
NP_001272328.1:p.Glu306Gln
|
|
NM_001285400.2:c.886G>C
|
NP_001272329.1:p.Glu296Gln
|
|
NM_001285401.2:c.880G>C
|
NP_001272330.1:p.Glu294Gln
|
|
NM_001285402.1:c.835G>C
|
NP_001272331.1:p.Glu279Gln
|
|
NM_014336.4:c.952G>C
|
NP_055151.3:p.Glu318Gln
|
|
NM_001033054.3:c.763G>C
|
NP_001028226.1:p.Glu255Gln
|
|
NM_001033055.3:c.772G>C
|
NP_001028227.1:p.Glu258Gln
|
|
NM_001285399.3:c.916G>C
|
NP_001272328.1:p.Glu306Gln
|
|
NM_001285400.3:c.886G>C
|
NP_001272329.1:p.Glu296Gln
|
|
NM_001285401.3:c.880G>C
|
NP_001272330.1:p.Glu294Gln
|
|
NM_001285402.2:c.835G>C
|
NP_001272331.1:p.Glu279Gln
|
|
NM_001285403.3:c.*923G>C
|
NP_001272332.1:n.*923G>C
|
|
NM_014336.5:c.952G>C
MANE Select
|
NP_055151.3:p.Glu318Gln
|
|
NM_001285403.4:c.*923G>C
|
NP_001272332.1:n.*923G>C
|
|