ENST00000346342.8:c.757G>C
MANE Select
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ENSP00000329546.4:p.Glu253Gln
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ENST00000346342.7:c.757G>C
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ENSP00000329546.3:p.Glu253Gln
|
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ENST00000375581.3:c.823G>C
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ENSP00000364731.3:p.Glu275Gln
|
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ENST00000541084.5:c.571G>C
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ENSP00000442051.2:p.Glu191Gln
|
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NM_000131.4:c.823G>C , LRG_554t1:c.823G>C
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NP_000122.1:p.Glu275Gln
|
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NM_001267554.1:c.571G>C
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NP_001254483.1:p.Glu191Gln
|
|
NM_019616.3:c.757G>C , LRG_554t2:c.757G>C
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NP_062562.1:p.Glu253Gln
|
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NR_051961.1:n.844G>C
|
|
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XM_006719963.2:c.616G>C
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XP_006720026.1:p.Glu206Gln
|
|
XM_011537474.1:c.865G>C
|
XP_011535776.1:p.Glu289Gln
|
|
XM_011537475.1:c.679G>C
|
XP_011535777.1:p.Glu227Gln
|
|
XM_011537476.1:c.517G>C
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XP_011535778.1:p.Glu173Gln
|
|
XM_011537477.1:c.826G>C
|
XP_011535779.1:p.Glu276Gln
|
|
XM_006719963.3:c.661G>C
|
XP_006720026.2:p.Glu221Gln
|
|
XM_011537474.2:c.910G>C
|
XP_011535776.2:p.Glu304Gln
|
|
XM_011537475.2:c.724G>C
|
XP_011535777.2:p.Glu242Gln
|
|
XM_011537476.2:c.517G>C
|
XP_011535778.1:p.Glu173Gln
|
|
NM_019616.4:c.757G>C
MANE Select
|
NP_062562.1:p.Glu253Gln
|
|
NR_051961.2:n.841G>C
|
|
|
NM_001267554.2:c.571G>C
|
NP_001254483.1:p.Glu191Gln
|
|