ENST00000262367.10:c.4440T>A
MANE Select
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ENSP00000262367.5:p.Asp1480Glu
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ENST00000262367.9:c.4440T>A
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ENSP00000262367.5:p.Asp1480Glu
|
|
ENST00000382070.7:c.4326T>A
|
ENSP00000371502.3:p.Asp1442Glu
|
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ENST00000570939.2:c.3075T>A
|
ENSP00000461002.2:p.Asp1025Glu
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ENST00000571763.5:n.230T>A
|
|
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ENST00000574740.1:n.261T>A
|
|
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ENST00000576720.1:n.3263T>A
|
|
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NM_001079846.1:c.4326T>A
|
NP_001073315.1:p.Asp1442Glu
|
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NM_004380.2:c.4440T>A
|
NP_004371.2:p.Asp1480Glu
|
|
XM_005255124.3:c.4395T>A
|
XP_005255181.1:p.Asp1465Glu
|
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XM_005255125.3:c.4023T>A
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XP_005255182.1:p.Asp1341Glu
|
|
XM_006720848.2:c.4179T>A
|
XP_006720911.1:p.Asp1393Glu
|
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XM_011522380.1:c.4386T>A
|
XP_011520682.1:p.Asp1462Glu
|
|
XM_011522381.1:c.3687T>A
|
XP_011520683.1:p.Asp1229Glu
|
|
XM_005255124.4:c.4395T>A
|
XP_005255181.1:p.Asp1465Glu
|
|
XM_005255125.4:c.4023T>A
|
XP_005255182.1:p.Asp1341Glu
|
|
XM_006720848.3:c.4179T>A
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XP_006720911.1:p.Asp1393Glu
|
|
XM_011522381.2:c.3687T>A
|
XP_011520683.1:p.Asp1229Glu
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|
XM_017022944.1:c.4434T>A
|
XP_016878433.1:p.Asp1478Glu
|
|
NM_004380.3:c.4440T>A
MANE Select
|
NP_004371.2:p.Asp1480Glu
|
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