ENST00000346342.8:c.758A>T
MANE Select
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ENSP00000329546.4:p.Glu253Val
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ENST00000346342.7:c.758A>T
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ENSP00000329546.3:p.Glu253Val
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ENST00000375581.3:c.824A>T
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ENSP00000364731.3:p.Glu275Val
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ENST00000541084.5:c.572A>T
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ENSP00000442051.2:p.Glu191Val
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NM_000131.4:c.824A>T , LRG_554t1:c.824A>T
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NP_000122.1:p.Glu275Val
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NM_001267554.1:c.572A>T
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NP_001254483.1:p.Glu191Val
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NM_019616.3:c.758A>T , LRG_554t2:c.758A>T
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NP_062562.1:p.Glu253Val
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NR_051961.1:n.845A>T
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|
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XM_006719963.2:c.617A>T
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XP_006720026.1:p.Glu206Val
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XM_011537474.1:c.866A>T
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XP_011535776.1:p.Glu289Val
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XM_011537475.1:c.680A>T
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XP_011535777.1:p.Glu227Val
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XM_011537476.1:c.518A>T
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XP_011535778.1:p.Glu173Val
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XM_011537477.1:c.827A>T
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XP_011535779.1:p.Glu276Val
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XM_006719963.3:c.662A>T
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XP_006720026.2:p.Glu221Val
|
|
XM_011537474.2:c.911A>T
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XP_011535776.2:p.Glu304Val
|
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XM_011537475.2:c.725A>T
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XP_011535777.2:p.Glu242Val
|
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XM_011537476.2:c.518A>T
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XP_011535778.1:p.Glu173Val
|
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NM_019616.4:c.758A>T
MANE Select
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NP_062562.1:p.Glu253Val
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NR_051961.2:n.842A>T
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NM_001267554.2:c.572A>T
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NP_001254483.1:p.Glu191Val
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|