ENST00000301761.7:c.394T>G
MANE Select
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ENSP00000301761.3:p.Phe132Val
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|
ENST00000301761.6:c.394T>G
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ENSP00000301761.2:p.Phe132Val
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ENST00000359614.9:c.*102T>G
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ENSP00000352630.5:n.*102T>G
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ENST00000536670.5:n.396+7851T>G
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|
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ENST00000537782.5:c.*40T>G
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ENSP00000469951.1:n.*40T>G
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ENST00000538594.5:c.370+7851T>G
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ENSP00000440939.1:n.370+7851T>G
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ENST00000541135.5:c.377+7844T>G
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ENSP00000443130.1:n.377+7844T>G
|
|
ENST00000542074.1:c.60T>G
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ENSP00000469670.1:p.Tyr20Ter
|
|
ENST00000542794.5:c.*396T>G
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ENSP00000439983.1:n.*396T>G
|
|
ENST00000543044.2:c.358T>G
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ENSP00000440219.1:p.Phe120Val
|
|
ENST00000543265.1:c.*17T>G
|
ENSP00000443660.1:n.*17T>G
|
|
ENST00000544025.5:n.465+7851T>G
|
|
|
ENST00000544801.5:c.370+7851T>G
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ENSP00000442581.1:n.370+7851T>G
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|
ENST00000544880.1:n.374+7851T>G
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|
|
NM_017841.2:c.394T>G , LRG_519t1:c.394T>G
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NP_060311.1:p.Phe132Val
|
|
NM_017841.4:c.394T>G
MANE Select
|
NP_060311.1:p.Phe132Val
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