ENST00000436784.7:c.1306A>G
MANE Select
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ENSP00000389175.2:p.Arg436Gly
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ENST00000305690.12:c.*425A>G
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ENSP00000301965.9:n.*425A>G
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ENST00000436784.6:c.1306A>G
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ENSP00000389175.2:p.Arg436Gly
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ENST00000461183.5:c.764-186A>G
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ENSP00000417264.1:n.764-186A>G
|
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ENST00000471180.5:c.635-186A>G
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ENSP00000417526.1:n.635-186A>G
|
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ENST00000473032.5:c.530-186A>G
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ENSP00000418951.1:n.530-186A>G
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ENST00000477382.1:c.*425A>G
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ENSP00000419008.1:n.*425A>G
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ENST00000486393.5:c.*669A>G
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ENSP00000419868.1:n.*669A>G
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ENST00000489173.1:n.1600A>G
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|
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NM_001144951.1:c.*425A>G
|
NP_001138423.1:n.*425A>G
|
|
NM_145262.3:c.1306A>G
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NP_660305.2:p.Arg436Gly
|
|
NR_026699.1:n.1404A>G
|
|
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NR_026700.1:n.696-186A>G
|
|
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NR_026701.1:n.1402A>G
|
|
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NR_026702.1:n.626-186A>G
|
|
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XM_005264878.2:c.*425A>G
|
XP_005264935.1:n.*425A>G
|
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XR_245095.2:n.2743-186A>G
|
|
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XM_017005730.1:c.925A>G
|
XP_016861219.1:p.Arg309Gly
|
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XM_024453351.1:c.1306A>G
|
XP_024309119.1:p.Arg436Gly
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XM_024453352.1:c.*425A>G
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XP_024309120.1:n.*425A>G
|
|
XR_001740022.2:n.3208A>G
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|
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XR_001740023.2:n.2918-186A>G
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|
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XR_245095.4:n.2744-186A>G
|
|
|
NM_145262.4:c.1306A>G
MANE Select
|
NP_660305.2:p.Arg436Gly
|
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NR_026699.2:n.1396A>G
|
|
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NR_026700.2:n.688-186A>G
|
|
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NR_026701.2:n.1394A>G
|
|
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NR_026702.2:n.618-186A>G
|
|
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NM_001144951.2:c.*425A>G
|
NP_001138423.1:n.*425A>G
|
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