ENST00000356141.9:c.1762G>T
MANE Select
|
ENSP00000348460.4:p.Glu588Ter
|
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ENST00000551634.6:c.1771G>T
|
ENSP00000448373.2:p.Glu591Ter
|
|
ENST00000680362.1:c.1662G>T
|
|
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ENST00000681323.1:c.793+2488G>T
|
|
|
ENST00000346562.6:c.1666G>T
|
ENSP00000319610.5:p.Glu556Ter
|
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ENST00000356141.8:c.1762G>T
|
ENSP00000348460.4:p.Glu588Ter
|
|
ENST00000357798.9:c.1723G>T
|
ENSP00000350446.5:p.Glu575Ter
|
|
ENST00000548645.5:c.1672G>T
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ENSP00000448916.1:p.Glu558Ter
|
|
ENST00000551492.5:c.1777G>T
|
ENSP00000450392.1:p.Glu593Ter
|
|
ENST00000551634.5:c.1684G>T
|
ENSP00000448373.1:p.Glu562Ter
|
|
NM_001164749.1:c.1762G>T
|
NP_001158221.1:p.Glu588Ter
|
|
NM_001165893.1:c.1672G>T
|
NP_001159365.1:p.Glu558Ter
|
|
NM_022123.2:c.1666G>T
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NP_071406.1:p.Glu556Ter
|
|
NM_173159.2:c.1723G>T
|
NP_775182.1:p.Glu575Ter
|
|
XM_005267991.2:c.1783G>T
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XP_005268048.1:p.Glu595Ter
|
|
XM_005267992.2:c.1777G>T
|
XP_005268049.1:p.Glu593Ter
|
|
XM_005267993.2:c.1723G>T
|
XP_005268050.1:p.Glu575Ter
|
|
XM_011537067.1:c.1813G>T
|
XP_011535369.1:p.Glu605Ter
|
|
XM_011537068.1:c.1804G>T
|
XP_011535370.1:p.Glu602Ter
|
|
XM_011537069.1:c.1774G>T
|
XP_011535371.1:p.Glu592Ter
|
|
XM_011537070.1:c.1717G>T
|
XP_011535372.1:p.Glu573Ter
|
|
XM_011537071.1:c.1684G>T
|
XP_011535373.1:p.Glu562Ter
|
|
XM_011537072.1:c.1663G>T
|
XP_011535374.1:p.Glu555Ter
|
|
XM_011537073.1:c.1456G>T
|
XP_011535375.1:p.Glu486Ter
|
|
XM_011537074.1:c.1456G>T
|
XP_011535376.1:p.Glu486Ter
|
|
XM_005267991.3:c.1870G>T
|
XP_005268048.2:p.Glu624Ter
|
|
XM_005267992.3:c.1864G>T
|
XP_005268049.2:p.Glu622Ter
|
|
XM_011537067.2:c.1813G>T
|
XP_011535369.1:p.Glu605Ter
|
|
XM_011537069.2:c.1861G>T
|
XP_011535371.2:p.Glu621Ter
|
|
XM_011537070.2:c.1717G>T
|
XP_011535372.1:p.Glu573Ter
|
|
XM_011537071.2:c.1771G>T
|
XP_011535373.2:p.Glu591Ter
|
|
XM_011537072.2:c.1663G>T
|
XP_011535374.1:p.Glu555Ter
|
|
XM_017021582.1:c.1921G>T
|
XP_016877071.1:p.Glu641Ter
|
|
XM_017021583.1:c.1912G>T
|
XP_016877072.1:p.Glu638Ter
|
|
XM_017021584.1:c.1831G>T
|
XP_016877073.1:p.Glu611Ter
|
|
XM_017021585.1:c.1780G>T
|
XP_016877074.1:p.Glu594Ter
|
|
XM_017021586.1:c.1456G>T
|
XP_016877075.1:p.Glu486Ter
|
|
XM_017021587.1:c.1456G>T
|
XP_016877076.1:p.Glu486Ter
|
|
XM_017021588.1:c.1456G>T
|
XP_016877077.1:p.Glu486Ter
|
|
NM_001164749.2:c.1762G>T
MANE Select
|
NP_001158221.1:p.Glu588Ter
|
|
NM_001165893.2:c.1672G>T
|
NP_001159365.1:p.Glu558Ter
|
|
NM_022123.3:c.1666G>T
|
NP_071406.1:p.Glu556Ter
|
|
NM_173159.3:c.1723G>T
|
NP_775182.1:p.Glu575Ter
|
|
NM_001394988.1:c.1717G>T
|
NP_001381917.1:p.Glu573Ter
|
|
NM_001394989.1:c.1663G>T
|
NP_001381918.1:p.Glu555Ter
|
|