ENST00000298910.12:c.4890T>A
MANE Select
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ENSP00000298910.7:p.Asp1630Glu
|
|
ENST00000679360.1:c.*3799T>A
|
ENSP00000505368.1:n.*3799T>A
|
|
ENST00000679532.1:c.664T>A
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|
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ENST00000680018.1:c.335T>A
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ENSP00000505347.1:n.335T>A
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ENST00000680422.1:c.535T>A
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|
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ENST00000680425.1:c.183-984T>A
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ENSP00000506459.1:n.183-984T>A
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ENST00000680453.1:c.473-984T>A
|
|
|
ENST00000680790.1:c.4635T>A
|
ENSP00000505335.1:p.Asp1545Glu
|
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ENST00000681136.1:n.874T>A
|
|
|
ENST00000681696.1:c.573T>A
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ENSP00000505871.1:p.Asp191Glu
|
|
ENST00000298910.11:c.4890T>A
|
ENSP00000298910.7:p.Asp1630Glu
|
|
ENST00000430804.5:c.2186T>A
|
|
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ENST00000479187.5:n.1571T>A
|
|
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ENST00000481256.1:n.549T>A
|
|
|
NM_198578.3:c.4890T>A
|
NP_940980.3:p.Asp1630Glu
|
|
XM_005268629.2:c.4890T>A
|
XP_005268686.1:p.Asp1630Glu
|
|
XM_011537877.1:c.4890T>A
|
XP_011536179.1:p.Asp1630Glu
|
|
XM_011537878.1:c.4890T>A
|
XP_011536180.1:p.Asp1630Glu
|
|
XM_011537879.1:c.3687T>A
|
XP_011536181.1:p.Asp1229Glu
|
|
XM_011537881.1:c.4828-984T>A
|
XP_011536183.1:n.4828-984T>A
|
|
XM_005268629.4:c.4890T>A
|
XP_005268686.1:p.Asp1630Glu
|
|
XM_011537877.3:c.4890T>A
|
XP_011536179.1:p.Asp1630Glu
|
|
XM_011537881.3:c.4828-984T>A
|
XP_011536183.1:n.4828-984T>A
|
|
XM_017018787.1:c.1806T>A
|
XP_016874276.1:p.Asp602Glu
|
|
XM_017018788.2:c.1152T>A
|
XP_016874277.1:p.Asp384Glu
|
|
XM_024448833.1:c.3687T>A
|
XP_024304601.1:p.Asp1229Glu
|
|
XR_001748574.2:n.5258T>A
|
|
|
NM_198578.4:c.4890T>A
MANE Select
|
NP_940980.4:p.Asp1630Glu
|
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