ENST00000422447.8:c.886G>A
MANE Select
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ENSP00000395337.3:p.Gly296Arg
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ENST00000227157.8:c.*36G>A
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ENSP00000227157.4:n.*36G>A
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ENST00000375710.7:n.1753G>A
|
|
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ENST00000379412.9:c.886G>A
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ENSP00000368722.5:p.Gly296Arg
|
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ENST00000396222.6:c.688-71G>A
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ENSP00000379524.2:n.688-71G>A
|
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ENST00000422447.7:c.886G>A
|
ENSP00000395337.3:p.Gly296Arg
|
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ENST00000430553.6:c.712G>A
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ENSP00000406172.2:p.Gly238Arg
|
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ENST00000538451.1:n.773G>A
|
|
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ENST00000540430.5:c.973G>A
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ENSP00000445175.1:p.Gly325Arg
|
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ENST00000542179.1:c.886G>A
|
ENSP00000445331.1:p.Gly296Arg
|
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ENST00000545215.5:c.*630G>A
|
ENSP00000442637.1:n.*630G>A
|
|
NM_001135239.1:c.712G>A
|
NP_001128711.1:p.Gly238Arg
|
|
NM_001165414.1:c.973G>A
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NP_001158886.1:p.Gly325Arg
|
|
NM_001165415.1:c.688-71G>A
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NP_001158887.1:n.688-71G>A
|
|
NM_001165416.1:c.*36G>A
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NP_001158888.1:n.*36G>A
|
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NM_005566.3:c.886G>A
|
NP_005557.1:p.Gly296Arg
|
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NR_028500.1:n.1040G>A
|
|
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NM_005566.4:c.886G>A
MANE Select
|
NP_005557.1:p.Gly296Arg
|
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NM_001165415.2:c.688-71G>A
|
NP_001158887.1:n.688-71G>A
|
|
NM_001135239.2:c.712G>A
|
NP_001128711.1:p.Gly238Arg
|
|
NM_001165414.2:c.973G>A
|
NP_001158886.1:p.Gly325Arg
|
|
NM_001165416.2:c.*36G>A
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NP_001158888.1:n.*36G>A
|
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NR_028500.2:n.866G>A
|
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