ENST00000356518.7:c.1704G>T
MANE Select
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ENSP00000348912.3:p.Gly568=
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ENST00000350009.6:c.1704G>T
|
ENSP00000322550.5:p.Gly568=
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|
ENST00000356518.6:c.1704G>T
|
ENSP00000348912.2:p.Gly568=
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|
ENST00000379861.8:c.1704G>T
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ENSP00000369190.4:p.Gly568=
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ENST00000466620.5:n.1343G>T
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|
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ENST00000617732.1:c.*632-422G>T
|
ENSP00000483343.1:n.*632-422G>T
|
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ENST00000619289.4:c.1344G>T
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ENSP00000484600.1:p.Gly448=
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NM_001282447.1:c.1704G>T
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NP_001269376.1:p.Gly568=
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|
NM_025220.3:c.1704G>T
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NP_079496.1:p.Gly568=
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|
NM_153202.2:c.1704G>T
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NP_694882.1:p.Gly568=
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|
XM_005260843.1:c.1743G>T
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XP_005260900.1:p.Gly581=
|
|
XM_006723639.1:c.1743G>T
|
XP_006723702.1:p.Gly581=
|
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XM_006723640.1:c.1734G>T
|
XP_006723703.1:p.Gly578=
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|
XM_011529366.1:c.1740G>T
|
XP_011527668.1:p.Gly580=
|
|
XM_011529367.1:c.1701G>T
|
XP_011527669.1:p.Gly567=
|
|
XM_011529368.1:c.1743G>T
|
XP_011527670.1:p.Gly581=
|
|
XM_011529369.1:c.1711G>T
|
XP_011527671.1:p.Glu571Ter
|
|
XM_011529370.1:c.1711G>T
|
XP_011527672.1:p.Glu571Ter
|
|
XM_011529373.1:c.741G>T
|
XP_011527675.1:p.Gly247=
|
|
XR_937151.1:n.1847G>T
|
|
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XR_937152.1:n.1847G>T
|
|
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XR_937153.1:n.1728G>T
|
|
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XR_937154.1:n.1728G>T
|
|
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XR_937155.1:n.1649G>T
|
|
|
XR_937157.1:n.1651G>T
|
|
|
NM_001282447.2:c.1704G>T
|
NP_001269376.1:p.Gly568=
|
|
NM_025220.4:c.1704G>T
|
NP_079496.1:p.Gly568=
|
|
NM_153202.3:c.1704G>T
|
NP_694882.1:p.Gly568=
|
|
XM_011529373.2:c.741G>T
|
XP_011527675.1:p.Gly247=
|
|
XR_001754405.1:n.1815G>T
|
|
|
XR_002958534.1:n.1924G>T
|
|
|
NM_001282447.3:c.1704G>T
|
NP_001269376.1:p.Gly568=
|
|
NM_025220.5:c.1704G>T
MANE Select
|
NP_079496.1:p.Gly568=
|
|
NM_153202.4:c.1704G>T
|
NP_694882.1:p.Gly568=
|
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