ENST00000261772.13:c.2073T>C
MANE Select
|
ENSP00000261772.8:p.Pro691=
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ENST00000564359.6:n.2150+843T>C
|
|
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ENST00000565361.3:c.2073T>C
|
ENSP00000455360.3:p.Pro691=
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ENST00000674512.1:c.2052T>C
|
ENSP00000501613.1:p.Pro684=
|
|
ENST00000674652.1:c.*1862T>C
|
ENSP00000502620.1:n.*1862T>C
|
|
ENST00000674691.1:c.2073T>C
|
ENSP00000502247.1:p.Pro691=
|
|
ENST00000674768.1:c.*328T>C
|
ENSP00000501679.1:n.*328T>C
|
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ENST00000674811.1:c.*266T>C
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ENSP00000502055.1:n.*266T>C
|
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ENST00000674848.1:n.2122T>C
|
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ENST00000674962.1:n.2231T>C
|
|
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ENST00000674963.1:c.2073T>C
|
ENSP00000501924.1:p.Pro691=
|
|
ENST00000675035.1:c.2073T>C
|
ENSP00000502712.1:p.Pro691=
|
|
ENST00000675045.1:c.2100T>C
|
ENSP00000502014.1:p.Pro700=
|
|
ENST00000675120.1:c.*383T>C
|
ENSP00000502823.1:n.*383T>C
|
|
ENST00000675133.1:c.2046T>C
|
ENSP00000502230.1:p.Pro682=
|
|
ENST00000675270.1:n.2208T>C
|
|
|
ENST00000675297.1:c.*425T>C
|
ENSP00000502753.1:n.*425T>C
|
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ENST00000675371.1:c.1992+843T>C
|
ENSP00000502645.1:n.1992+843T>C
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ENST00000675403.1:n.2993T>C
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ENST00000675569.1:c.*1307T>C
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ENSP00000502534.1:n.*1307T>C
|
|
ENST00000675643.1:c.2073T>C
|
ENSP00000502797.1:p.Pro691=
|
|
ENST00000675691.1:c.1944T>C
|
ENSP00000502196.1:p.Pro648=
|
|
ENST00000675751.1:c.*1100T>C
|
ENSP00000502277.1:n.*1100T>C
|
|
ENST00000675853.1:c.2073T>C
|
ENSP00000502367.1:p.Pro691=
|
|
ENST00000675917.1:n.2370T>C
|
|
|
ENST00000675953.1:c.1989T>C
|
ENSP00000502321.1:p.Pro663=
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|
ENST00000675986.1:n.2231T>C
|
|
|
ENST00000676004.1:c.*2072T>C
|
ENSP00000502765.1:n.*2072T>C
|
|
ENST00000676040.1:c.*1307T>C
|
ENSP00000502108.1:n.*1307T>C
|
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ENST00000676168.1:c.1992+843T>C
|
ENSP00000502479.1:n.1992+843T>C
|
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ENST00000676209.1:c.*425T>C
|
ENSP00000502052.1:n.*425T>C
|
|
ENST00000676211.1:c.*1100T>C
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ENSP00000502726.1:n.*1100T>C
|
|
ENST00000676212.1:c.2073T>C
|
ENSP00000501853.1:p.Pro691=
|
|
ENST00000676247.1:c.*425T>C
|
ENSP00000502699.1:n.*425T>C
|
|
ENST00000261772.12:c.2073T>C
|
ENSP00000261772.7:p.Pro691=
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|
ENST00000564359.5:n.488+843T>C
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ENST00000565361.2:c.418T>C
|
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ENST00000569825.1:n.79T>C
|
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NM_001605.2:c.2073T>C , LRG_359t1:c.2073T>C
|
NP_001596.2:p.Pro691=
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|
XR_933220.1:n.2143+843T>C
|
|
|
XR_933220.3:n.2102+843T>C
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|
|
NM_001605.3:c.2073T>C
MANE Select
|
NP_001596.2:p.Pro691=
|
|