ENST00000320185.7:c.353A>T
MANE Select
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ENSP00000321797.2:p.Glu118Val
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ENST00000618991.5:c.41A>T
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ENSP00000484420.1:p.Glu14Val
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ENST00000344255.8:c.320A>T
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ENSP00000340039.3:p.Glu107Val
|
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ENST00000320185.6:c.353A>T
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ENSP00000321797.2:p.Glu118Val
|
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ENST00000344255.7:c.320A>T
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ENSP00000340039.3:p.Glu107Val
|
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ENST00000346714.7:c.233A>T
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ENSP00000344306.3:p.Glu78Val
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ENST00000347978.2:c.266A>T
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ENSP00000321945.2:p.Glu89Val
|
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ENST00000469792.6:c.*317A>T
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ENSP00000473299.1:n.*317A>T
|
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ENST00000485728.1:n.229A>T
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|
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ENST00000618991.4:c.41A>T
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ENSP00000484420.1:p.Glu14Val
|
|
NM_001206389.1:c.41A>T
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NP_001193318.1:p.Glu14Val
|
|
NM_006119.4:c.266A>T
|
NP_006110.1:p.Glu89Val
|
|
NM_033163.3:c.353A>T
|
NP_149353.1:p.Glu118Val
|
|
NM_033164.3:c.320A>T
|
NP_149354.1:p.Glu107Val
|
|
NM_033165.3:c.233A>T
|
NP_149355.1:p.Glu78Val
|
|
XM_011539509.1:c.275A>T
|
XP_011537811.1:p.Glu92Val
|
|
XR_946251.1:n.335T>A
|
|
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XR_946252.1:n.266T>A
|
|
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XR_946253.1:n.264T>A
|
|
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XR_946252.2:n.356T>A
|
|
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XR_946253.2:n.354T>A
|
|
|
NM_006119.5:c.266A>T
|
NP_006110.1:p.Glu89Val
|
|
NM_033163.4:c.353A>T
|
NP_149353.1:p.Glu118Val
|
|
NM_033164.4:c.320A>T
|
NP_149354.1:p.Glu107Val
|
|
NM_033165.4:c.233A>T
|
NP_149355.1:p.Glu78Val
|
|
NM_001206389.2:c.41A>T
|
NP_001193318.1:p.Glu14Val
|
|
NM_006119.6:c.266A>T
|
NP_006110.1:p.Glu89Val
|
|
NM_033163.5:c.353A>T
MANE Select
|
NP_149353.1:p.Glu118Val
|
|
NM_033165.5:c.233A>T
|
NP_149355.1:p.Glu78Val
|
|