ENST00000253122.10:c.1332G>A
MANE Select
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ENSP00000253122.5:p.Glu444=
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ENST00000253122.9:c.1332G>A
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ENSP00000253122.5:p.Glu444=
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ENST00000413787.1:c.261G>A
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ENSP00000400463.1:p.Glu87=
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ENST00000430077.6:c.987G>A
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ENSP00000403041.2:p.Glu329=
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ENST00000442457.1:c.386G>A
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ENST00000485324.1:n.1477G>A
|
|
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NM_001142805.1:c.1302G>A
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NP_001136277.1:p.Glu434=
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NM_001142806.1:c.987G>A
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NP_001136278.1:p.Glu329=
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NM_005629.3:c.1332G>A
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NP_005620.1:p.Glu444=
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NM_005629.4:c.1332G>A
MANE Select
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NP_005620.1:p.Glu444=
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NM_001142805.2:c.1302G>A
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NP_001136277.1:p.Glu434=
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