ENST00000554809.6:c.2783A>T
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ENSP00000450632.2:p.Glu928Val
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ENST00000555484.2:c.349A>T
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ENST00000556250.6:c.4364A>T
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ENSP00000452033.2:p.Glu1455Val
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ENST00000557110.2:c.349A>T
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ENST00000696642.1:c.*3382A>T
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ENSP00000512775.1:n.*3382A>T
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ENST00000696644.1:n.307A>T
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ENST00000696645.1:n.461A>T
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ENST00000696647.1:c.4571A>T
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ENSP00000512778.1:p.Glu1524Val
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ENST00000696648.1:c.*2596A>T
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ENSP00000512779.1:n.*2596A>T
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ENST00000696649.1:c.4415A>T
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ENSP00000512780.1:p.Glu1472Val
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ENST00000696650.1:n.4519A>T
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ENST00000696659.1:c.2569A>T
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ENST00000696663.1:c.3502A>T
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ENST00000696664.1:c.3403A>T
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ENST00000696665.1:c.349A>T
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ENST00000696675.1:c.*327A>T
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ENSP00000512799.1:n.*327A>T
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ENST00000696683.1:c.3388A>T
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ENST00000696684.1:c.3388A>T
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ENST00000696685.1:c.3388A>T
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ENST00000696686.1:n.1308A>T
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ENST00000267430.10:c.4571A>T
MANE Select
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ENSP00000267430.5:p.Glu1524Val
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ENST00000267430.9:c.4571A>T
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ENSP00000267430.5:p.Glu1524Val
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ENST00000542564.6:c.4493A>T
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ENSP00000442493.2:p.Glu1498Val
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ENST00000554809.5:c.1368A>T
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|
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ENST00000555013.1:n.404A>T
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ENST00000556250.5:c.3119A>T
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ENSP00000452033.1:p.Glu1040Val
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NM_001308133.1:c.4493A>T
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NP_001295062.1:p.Glu1498Val
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NM_020937.2:c.4571A>T , LRG_502t1:c.4571A>T
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NP_065988.1:p.Glu1524Val
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NM_020937.3:c.4571A>T
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NP_065988.1:p.Glu1524Val
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XM_011537034.1:c.4586A>T
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XP_011535336.1:p.Glu1529Val
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XM_011537035.1:c.4508A>T
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XP_011535337.1:p.Glu1503Val
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|
XM_011537036.1:c.4586A>T
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XP_011535338.1:p.Glu1529Val
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XM_011537037.1:c.2600A>T
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XP_011535339.1:p.Glu867Val
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XM_011537034.2:c.4586A>T
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XP_011535336.1:p.Glu1529Val
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XM_011537035.3:c.4508A>T
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XP_011535337.1:p.Glu1503Val
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XM_011537037.3:c.2600A>T
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XP_011535339.1:p.Glu867Val
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|
XM_017021523.1:c.4586A>T
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XP_016877012.1:p.Glu1529Val
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XM_017021524.2:c.3623A>T
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XP_016877013.1:p.Glu1208Val
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XM_017021525.2:c.3401A>T
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XP_016877014.1:p.Glu1134Val
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XM_017021526.2:c.3401A>T
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XP_016877015.1:p.Glu1134Val
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XM_017021527.1:c.3386A>T
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XP_016877016.1:p.Glu1129Val
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XR_001750470.1:n.4678A>T
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|
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XR_001750471.2:n.4663A>T
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|
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XR_001750472.1:n.4715A>T
|
|
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NM_020937.4:c.4571A>T
MANE Select
|
NP_065988.1:p.Glu1524Val
|
|
NM_001308133.2:c.4493A>T
|
NP_001295062.1:p.Glu1498Val
|
|