ENST00000452508.7:c.5567A>T
|
ENSP00000388058.2:p.Glu1856Val
|
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ENST00000713593.1:c.*5038A>T
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ENSP00000518889.1:n.*5038A>T
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|
ENST00000278616.9:c.5567A>T
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ENSP00000278616.4:p.Glu1856Val
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ENST00000683174.1:n.7051A>T
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|
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ENST00000683524.1:n.791A>T
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|
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ENST00000684152.1:n.1281A>T
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|
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ENST00000527805.6:c.*631A>T
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ENSP00000435747.2:n.*631A>T
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|
ENST00000675595.1:c.*631A>T
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ENSP00000502563.1:n.*631A>T
|
|
ENST00000675843.1:c.5567A>T
MANE Select
|
ENSP00000501606.1:p.Glu1856Val
|
|
ENST00000278616.8:c.5567A>T
|
ENSP00000278616.4:p.Glu1856Val
|
|
ENST00000452508.6:c.5567A>T
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ENSP00000388058.2:p.Glu1856Val
|
|
ENST00000524792.5:n.1782A>T
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|
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ENST00000529588.5:c.79A>T
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|
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ENST00000533690.5:n.971A>T
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|
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NM_000051.3:c.5567A>T , LRG_135t1:c.5567A>T
|
NP_000042.3:p.Glu1856Val
|
|
XM_005271561.3:c.5567A>T
|
XP_005271618.2:p.Glu1856Val
|
|
XM_005271562.3:c.5567A>T
|
XP_005271619.2:p.Glu1856Val
|
|
XM_006718843.2:c.5567A>T
|
XP_006718906.1:p.Glu1856Val
|
|
XM_006718845.1:c.1523A>T
|
XP_006718908.1:p.Glu508Val
|
|
XM_011542840.1:c.5567A>T
|
XP_011541142.1:p.Glu1856Val
|
|
XM_011542841.1:c.5567A>T
|
XP_011541143.1:p.Glu1856Val
|
|
XM_011542842.1:c.5402A>T
|
XP_011541144.1:p.Glu1801Val
|
|
XM_011542843.1:c.5567A>T
|
XP_011541145.1:p.Glu1856Val
|
|
XM_011542844.1:c.4523A>T
|
XP_011541146.1:p.Glu1508Val
|
|
XM_011542845.1:c.4259A>T
|
XP_011541147.1:p.Glu1420Val
|
|
XM_011542847.1:c.638A>T
|
XP_011541149.1:p.Glu213Val
|
|
NM_001351834.1:c.5567A>T
|
NP_001338763.1:p.Glu1856Val
|
|
XM_005271562.5:c.5567A>T
|
XP_005271619.2:p.Glu1856Val
|
|
XM_006718843.4:c.5567A>T
|
XP_006718906.1:p.Glu1856Val
|
|
XM_006718845.2:c.1523A>T
|
XP_006718908.1:p.Glu508Val
|
|
XM_011542840.3:c.5567A>T
|
XP_011541142.1:p.Glu1856Val
|
|
XM_011542842.3:c.5402A>T
|
XP_011541144.1:p.Glu1801Val
|
|
XM_011542843.2:c.5567A>T
|
XP_011541145.1:p.Glu1856Val
|
|
XM_011542844.3:c.4523A>T
|
XP_011541146.1:p.Glu1508Val
|
|
XM_011542845.2:c.4259A>T
|
XP_011541147.1:p.Glu1420Val
|
|
XM_017017789.2:c.5567A>T
|
XP_016873278.1:p.Glu1856Val
|
|
XM_017017790.2:c.5567A>T
|
XP_016873279.1:p.Glu1856Val
|
|
XM_017017791.1:c.5567A>T
|
XP_016873280.1:p.Glu1856Val
|
|
XR_002957150.1:n.6167A>T
|
|
|
NM_001351834.2:c.5567A>T
|
NP_001338763.1:p.Glu1856Val
|
|
NM_000051.4:c.5567A>T
MANE Select
|
NP_000042.3:p.Glu1856Val
|
|