ENST00000356141.9:c.1774C>G
MANE Select
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ENSP00000348460.4:p.Gln592Glu
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ENST00000551634.6:c.1783C>G
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ENSP00000448373.2:p.Gln595Glu
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ENST00000680362.1:c.1674C>G
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ENST00000681323.1:c.793+2500C>G
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ENST00000346562.6:c.1678C>G
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ENSP00000319610.5:p.Gln560Glu
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ENST00000356141.8:c.1774C>G
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ENSP00000348460.4:p.Gln592Glu
|
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ENST00000357798.9:c.1735C>G
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ENSP00000350446.5:p.Gln579Glu
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ENST00000548645.5:c.1684C>G
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ENSP00000448916.1:p.Gln562Glu
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ENST00000551492.5:c.1789C>G
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ENSP00000450392.1:p.Gln597Glu
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ENST00000551634.5:c.1696C>G
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ENSP00000448373.1:p.Gln566Glu
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NM_001164749.1:c.1774C>G
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NP_001158221.1:p.Gln592Glu
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|
NM_001165893.1:c.1684C>G
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NP_001159365.1:p.Gln562Glu
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|
NM_022123.2:c.1678C>G
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NP_071406.1:p.Gln560Glu
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|
NM_173159.2:c.1735C>G
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NP_775182.1:p.Gln579Glu
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|
XM_005267991.2:c.1795C>G
|
XP_005268048.1:p.Gln599Glu
|
|
XM_005267992.2:c.1789C>G
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XP_005268049.1:p.Gln597Glu
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XM_005267993.2:c.1735C>G
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XP_005268050.1:p.Gln579Glu
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XM_011537067.1:c.1825C>G
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XP_011535369.1:p.Gln609Glu
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XM_011537068.1:c.1816C>G
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XP_011535370.1:p.Gln606Glu
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XM_011537069.1:c.1786C>G
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XP_011535371.1:p.Gln596Glu
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XM_011537070.1:c.1729C>G
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XP_011535372.1:p.Gln577Glu
|
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XM_011537071.1:c.1696C>G
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XP_011535373.1:p.Gln566Glu
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XM_011537072.1:c.1675C>G
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XP_011535374.1:p.Gln559Glu
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|
XM_011537073.1:c.1468C>G
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XP_011535375.1:p.Gln490Glu
|
|
XM_011537074.1:c.1468C>G
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XP_011535376.1:p.Gln490Glu
|
|
XM_005267991.3:c.1882C>G
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XP_005268048.2:p.Gln628Glu
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XM_005267992.3:c.1876C>G
|
XP_005268049.2:p.Gln626Glu
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|
XM_011537067.2:c.1825C>G
|
XP_011535369.1:p.Gln609Glu
|
|
XM_011537069.2:c.1873C>G
|
XP_011535371.2:p.Gln625Glu
|
|
XM_011537070.2:c.1729C>G
|
XP_011535372.1:p.Gln577Glu
|
|
XM_011537071.2:c.1783C>G
|
XP_011535373.2:p.Gln595Glu
|
|
XM_011537072.2:c.1675C>G
|
XP_011535374.1:p.Gln559Glu
|
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XM_017021582.1:c.1933C>G
|
XP_016877071.1:p.Gln645Glu
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XM_017021583.1:c.1924C>G
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XP_016877072.1:p.Gln642Glu
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XM_017021584.1:c.1843C>G
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XP_016877073.1:p.Gln615Glu
|
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XM_017021585.1:c.1792C>G
|
XP_016877074.1:p.Gln598Glu
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XM_017021586.1:c.1468C>G
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XP_016877075.1:p.Gln490Glu
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XM_017021587.1:c.1468C>G
|
XP_016877076.1:p.Gln490Glu
|
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XM_017021588.1:c.1468C>G
|
XP_016877077.1:p.Gln490Glu
|
|
NM_001164749.2:c.1774C>G
MANE Select
|
NP_001158221.1:p.Gln592Glu
|
|
NM_001165893.2:c.1684C>G
|
NP_001159365.1:p.Gln562Glu
|
|
NM_022123.3:c.1678C>G
|
NP_071406.1:p.Gln560Glu
|
|
NM_173159.3:c.1735C>G
|
NP_775182.1:p.Gln579Glu
|
|
NM_001394988.1:c.1729C>G
|
NP_001381917.1:p.Gln577Glu
|
|
NM_001394989.1:c.1675C>G
|
NP_001381918.1:p.Gln559Glu
|
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