ENST00000327047.6:c.111T>A
MANE Select
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ENSP00000322280.1:p.Thr37=
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ENST00000468836.2:c.87T>A
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ENSP00000419892.2:p.Thr29=
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ENST00000327047.5:c.111T>A
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ENSP00000322280.1:p.Thr37=
|
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ENST00000328863.8:c.111T>A
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ENSP00000329158.4:p.Thr37=
|
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ENST00000468836.1:c.-290T>A
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ENSP00000419892.1:n.-290T>A
|
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ENST00000472224.1:n.117T>A
|
|
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NM_001195794.1:c.111T>A , LRG_700t1:c.111T>A
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NP_001182723.1:p.Thr37=
|
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NM_001256819.1:c.111T>A
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NP_001243748.1:p.Thr37=
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NM_174878.2:c.111T>A
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NP_777367.1:p.Thr37=
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NR_046380.2:n.402T>A
|
|
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XR_924167.1:n.423T>A
|
|
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NM_001256819.2:c.111T>A
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NP_001243748.1:p.Thr37=
|
|
NM_174878.3:c.111T>A
MANE Select
|
NP_777367.1:p.Thr37=
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NR_046380.3:n.130T>A
|
|
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