ENST00000232607.7:c.395T>C
MANE Select
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ENSP00000232607.2:p.Val132Ala
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|
ENST00000232607.6:c.395T>C
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ENSP00000232607.2:p.Val132Ala
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|
ENST00000460034.5:c.*139T>C
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ENSP00000420409.1:n.*139T>C
|
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ENST00000462091.5:c.*67T>C
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ENSP00000417893.1:n.*67T>C
|
|
ENST00000467167.5:c.*293T>C
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ENSP00000419618.1:n.*293T>C
|
|
ENST00000474588.5:c.311-263T>C
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ENSP00000420348.1:n.311-263T>C
|
|
ENST00000479719.5:c.395T>C
|
ENSP00000420754.1:p.Val132Ala
|
|
ENST00000497791.5:c.*67T>C
|
ENSP00000419121.1:n.*67T>C
|
|
ENST00000498715.1:n.113T>C
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|
|
NM_000373.3:c.395T>C
|
NP_000364.1:p.Val132Ala
|
|
NR_033434.1:n.347T>C
|
|
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NR_033437.1:n.600T>C
|
|
|
XR_001740253.2:n.425T>C
|
|
|
NM_000373.4:c.395T>C
MANE Select
|
NP_000364.1:p.Val132Ala
|
|
NR_033434.2:n.261T>C
|
|
|
NR_033437.2:n.514T>C
|
|
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