ENST00000261208.8:c.809A>T
MANE Select
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ENSP00000261208.3:p.Glu270Val
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ENST00000261208.7:c.809A>T
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ENSP00000261208.3:p.Glu270Val
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ENST00000538703.5:c.809A>T
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ENSP00000440861.1:p.Glu270Val
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ENST00000541929.5:c.185A>T
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ENSP00000446364.1:p.Glu62Val
|
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ENST00000544080.6:c.*238A>T
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ENSP00000439385.2:n.*238A>T
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ENST00000546999.5:c.*238A>T
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ENSP00000447675.1:n.*238A>T
|
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ENST00000549376.1:n.202A>T
|
|
|
ENST00000551562.1:n.69A>T
|
|
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ENST00000552509.5:c.773A>T
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ENSP00000450372.1:p.Glu258Val
|
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NM_001258333.1:c.185A>T
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NP_001245262.1:p.Glu62Val
|
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NM_001258334.1:c.809A>T
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NP_001245263.1:p.Glu270Val
|
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NM_002108.3:c.809A>T
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NP_002099.1:p.Glu270Val
|
|
XM_011538249.1:c.4-2199A>T
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XP_011536551.1:n.4-2199A>T
|
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XM_011538249.2:c.4-2199A>T
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XP_011536551.1:n.4-2199A>T
|
|
NM_002108.4:c.809A>T
MANE Select
|
NP_002099.1:p.Glu270Val
|
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NM_001258334.2:c.809A>T
|
NP_001245263.1:p.Glu270Val
|
|
NM_001258333.2:c.185A>T
|
NP_001245262.1:p.Glu62Val
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