ENST00000381129.8:c.949G>T
MANE Select
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ENSP00000370521.3:p.Glu317Ter
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ENST00000250087.9:c.760G>T
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ENSP00000250087.5:p.Glu254Ter
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ENST00000381128.2:c.*821G>T
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ENSP00000370520.2:n.*821G>T
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ENST00000381129.7:c.949G>T
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ENSP00000370521.3:p.Glu317Ter
|
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ENST00000570466.5:c.883G>T
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ENSP00000461287.1:p.Glu295Ter
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ENST00000570584.5:c.251+8253G>T
|
|
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ENST00000574506.5:c.913G>T
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ENSP00000458456.1:p.Glu305Ter
|
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ENST00000575265.5:c.*920G>T
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ENSP00000459673.1:n.*920G>T
|
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ENST00000576307.5:c.769G>T
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ENSP00000459522.1:p.Glu257Ter
|
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ENST00000576776.5:c.877G>T
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ENSP00000460827.1:p.Glu293Ter
|
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ENST00000621374.4:c.948G>T
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ENSP00000481337.1:p.Arg316Ser
|
|
NM_001033054.2:c.760G>T
|
NP_001028226.1:p.Glu254Ter
|
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NM_001033055.2:c.769G>T
|
NP_001028227.1:p.Glu257Ter
|
|
NM_001285399.2:c.913G>T
|
NP_001272328.1:p.Glu305Ter
|
|
NM_001285400.2:c.883G>T
|
NP_001272329.1:p.Glu295Ter
|
|
NM_001285401.2:c.877G>T
|
NP_001272330.1:p.Glu293Ter
|
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NM_001285402.1:c.832G>T
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NP_001272331.1:p.Glu278Ter
|
|
NM_014336.4:c.949G>T
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NP_055151.3:p.Glu317Ter
|
|
NM_001033054.3:c.760G>T
|
NP_001028226.1:p.Glu254Ter
|
|
NM_001033055.3:c.769G>T
|
NP_001028227.1:p.Glu257Ter
|
|
NM_001285399.3:c.913G>T
|
NP_001272328.1:p.Glu305Ter
|
|
NM_001285400.3:c.883G>T
|
NP_001272329.1:p.Glu295Ter
|
|
NM_001285401.3:c.877G>T
|
NP_001272330.1:p.Glu293Ter
|
|
NM_001285402.2:c.832G>T
|
NP_001272331.1:p.Glu278Ter
|
|
NM_001285403.3:c.*920G>T
|
NP_001272332.1:n.*920G>T
|
|
NM_014336.5:c.949G>T
MANE Select
|
NP_055151.3:p.Glu317Ter
|
|
NM_001285403.4:c.*920G>T
|
NP_001272332.1:n.*920G>T
|
|