ENST00000232607.7:c.633T>A
MANE Select
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ENSP00000232607.2:p.His211Gln
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|
ENST00000232607.6:c.633T>A
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ENSP00000232607.2:p.His211Gln
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|
ENST00000460034.5:c.*377T>A
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ENSP00000420409.1:n.*377T>A
|
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ENST00000462091.5:c.*305T>A
|
ENSP00000417893.1:n.*305T>A
|
|
ENST00000467167.5:c.*531T>A
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ENSP00000419618.1:n.*531T>A
|
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ENST00000474588.5:c.311-25T>A
|
ENSP00000420348.1:n.311-25T>A
|
|
ENST00000479719.5:c.633T>A
|
ENSP00000420754.1:p.His211Gln
|
|
ENST00000497791.5:c.*305T>A
|
ENSP00000419121.1:n.*305T>A
|
|
ENST00000498715.1:n.351T>A
|
|
|
NM_000373.3:c.633T>A
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NP_000364.1:p.His211Gln
|
|
NR_033434.1:n.585T>A
|
|
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NR_033437.1:n.838T>A
|
|
|
XR_001740253.2:n.663T>A
|
|
|
NM_000373.4:c.633T>A
MANE Select
|
NP_000364.1:p.His211Gln
|
|
NR_033434.2:n.499T>A
|
|
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NR_033437.2:n.752T>A
|
|
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