ENST00000576892.8:c.527A>C
MANE Select
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ENSP00000461135.1:p.Asp176Ala
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ENST00000429336.5:c.193+1911A>C
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ENST00000440428.5:c.527A>C
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ENSP00000402949.2:p.Asp176Ala
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ENST00000482182.3:c.401A>C
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ENSP00000466345.1:p.Asp134Ala
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ENST00000576892.7:c.527A>C
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ENSP00000461135.1:p.Asp176Ala
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ENST00000614850.1:c.277+3368A>C
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|
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ENST00000614851.4:c.348A>C
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ENST00000620088.4:c.*403A>C
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ENSP00000484108.1:n.*403A>C
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ENST00000621629.4:c.*403A>C
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ENSP00000478747.1:n.*403A>C
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ENST00000621817.1:c.*692A>C
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ENSP00000481634.1:n.*692A>C
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NM_001130997.2:c.527A>C
|
NP_001124469.1:p.Asp176Ala
|
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NM_152274.4:c.527A>C
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NP_689487.2:p.Asp176Ala
|
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XM_005277920.3:c.497A>C
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XP_005277977.1:p.Asp166Ala
|
|
XM_005277921.3:c.497A>C
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XP_005277978.1:p.Asp166Ala
|
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XM_011531213.1:c.401A>C
|
XP_011529515.1:p.Asp134Ala
|
|
XM_011531214.1:c.401A>C
|
XP_011529516.1:p.Asp134Ala
|
|
XM_011531215.1:c.401A>C
|
XP_011529517.1:p.Asp134Ala
|
|
XM_005277920.4:c.497A>C
|
XP_005277977.1:p.Asp166Ala
|
|
XM_005277921.4:c.497A>C
|
XP_005277978.1:p.Asp166Ala
|
|
XM_011531214.2:c.401A>C
|
XP_011529516.1:p.Asp134Ala
|
|
XM_011531215.2:c.401A>C
|
XP_011529517.1:p.Asp134Ala
|
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XR_002958810.1:n.2432A>C
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|
|
NM_152274.5:c.527A>C
MANE Select
|
NP_689487.2:p.Asp176Ala
|
|
NM_001130997.3:c.527A>C
|
NP_001124469.1:p.Asp176Ala
|
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