ENST00000346342.8:c.785G>A
MANE Select
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ENSP00000329546.4:p.Arg262Gln
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ENST00000346342.7:c.785G>A
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ENSP00000329546.3:p.Arg262Gln
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ENST00000375581.3:c.851G>A
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ENSP00000364731.3:p.Arg284Gln
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ENST00000541084.5:c.599G>A
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ENSP00000442051.2:p.Arg200Gln
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NM_000131.4:c.851G>A , LRG_554t1:c.851G>A
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NP_000122.1:p.Arg284Gln
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NM_001267554.1:c.599G>A
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NP_001254483.1:p.Arg200Gln
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NM_019616.3:c.785G>A , LRG_554t2:c.785G>A
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NP_062562.1:p.Arg262Gln
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NR_051961.1:n.872G>A
|
|
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XM_006719963.2:c.644G>A
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XP_006720026.1:p.Arg215Gln
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XM_011537474.1:c.893G>A
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XP_011535776.1:p.Arg298Gln
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XM_011537475.1:c.707G>A
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XP_011535777.1:p.Arg236Gln
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XM_011537476.1:c.545G>A
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XP_011535778.1:p.Arg182Gln
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XM_011537477.1:c.854G>A
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XP_011535779.1:p.Arg285Gln
|
|
XM_006719963.3:c.689G>A
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XP_006720026.2:p.Arg230Gln
|
|
XM_011537474.2:c.938G>A
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XP_011535776.2:p.Arg313Gln
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XM_011537475.2:c.752G>A
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XP_011535777.2:p.Arg251Gln
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XM_011537476.2:c.545G>A
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XP_011535778.1:p.Arg182Gln
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NM_019616.4:c.785G>A
MANE Select
|
NP_062562.1:p.Arg262Gln
|
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NR_051961.2:n.869G>A
|
|
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NM_001267554.2:c.599G>A
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NP_001254483.1:p.Arg200Gln
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