ENST00000356518.7:c.1659A>T
MANE Select
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ENSP00000348912.3:p.Gly553=
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ENST00000350009.6:c.1659A>T
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ENSP00000322550.5:p.Gly553=
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ENST00000356518.6:c.1659A>T
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ENSP00000348912.2:p.Gly553=
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ENST00000379861.8:c.1659A>T
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ENSP00000369190.4:p.Gly553=
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ENST00000466620.5:n.1298A>T
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|
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ENST00000617732.1:c.*632-467A>T
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ENSP00000483343.1:n.*632-467A>T
|
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ENST00000619289.4:c.1299A>T
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ENSP00000484600.1:p.Gly433=
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|
NM_001282447.1:c.1659A>T
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NP_001269376.1:p.Gly553=
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|
NM_025220.3:c.1659A>T
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NP_079496.1:p.Gly553=
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|
NM_153202.2:c.1659A>T
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NP_694882.1:p.Gly553=
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|
XM_005260843.1:c.1698A>T
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XP_005260900.1:p.Gly566=
|
|
XM_006723639.1:c.1698A>T
|
XP_006723702.1:p.Gly566=
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XM_006723640.1:c.1689A>T
|
XP_006723703.1:p.Gly563=
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XM_011529366.1:c.1695A>T
|
XP_011527668.1:p.Gly565=
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|
XM_011529367.1:c.1656A>T
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XP_011527669.1:p.Gly552=
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|
XM_011529368.1:c.1698A>T
|
XP_011527670.1:p.Gly566=
|
|
XM_011529369.1:c.1666A>T
|
XP_011527671.1:p.Lys556Ter
|
|
XM_011529370.1:c.1666A>T
|
XP_011527672.1:p.Lys556Ter
|
|
XM_011529373.1:c.696A>T
|
XP_011527675.1:p.Gly232=
|
|
XR_937151.1:n.1802A>T
|
|
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XR_937152.1:n.1802A>T
|
|
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XR_937153.1:n.1683A>T
|
|
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XR_937154.1:n.1683A>T
|
|
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XR_937155.1:n.1604A>T
|
|
|
XR_937157.1:n.1606A>T
|
|
|
NM_001282447.2:c.1659A>T
|
NP_001269376.1:p.Gly553=
|
|
NM_025220.4:c.1659A>T
|
NP_079496.1:p.Gly553=
|
|
NM_153202.3:c.1659A>T
|
NP_694882.1:p.Gly553=
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|
XM_011529373.2:c.696A>T
|
XP_011527675.1:p.Gly232=
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|
XR_001754405.1:n.1770A>T
|
|
|
XR_002958534.1:n.1879A>T
|
|
|
NM_001282447.3:c.1659A>T
|
NP_001269376.1:p.Gly553=
|
|
NM_025220.5:c.1659A>T
MANE Select
|
NP_079496.1:p.Gly553=
|
|
NM_153202.4:c.1659A>T
|
NP_694882.1:p.Gly553=
|
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