ENST00000692008.1:c.1128G>A
MANE Select
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ENSP00000509398.1:p.Glu376=
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ENST00000293308.11:c.1128G>A
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ENSP00000293308.6:p.Glu376=
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ENST00000546583.5:n.2318G>A
|
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ENST00000546897.5:c.1128G>A
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ENSP00000447402.1:p.Glu376=
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ENST00000547031.5:n.599G>A
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ENST00000550170.5:n.1666G>A
|
|
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ENST00000552150.5:c.1212G>A
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ENSP00000449404.1:p.Glu404=
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ENST00000552551.5:c.1128G>A
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ENSP00000447566.1:p.Glu376=
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NM_001256282.1:c.1212G>A
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NP_001243211.1:p.Glu404=
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NM_001256293.1:c.1128G>A
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NP_001243222.1:p.Glu376=
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NM_002273.3:c.1128G>A
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NP_002264.1:p.Glu376=
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NR_045962.1:n.1585G>A
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|
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NM_001256282.2:c.1212G>A
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NP_001243211.1:p.Glu404=
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NM_001256293.2:c.1128G>A
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NP_001243222.1:p.Glu376=
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NM_002273.4:c.1128G>A
MANE Select
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NP_002264.1:p.Glu376=
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NR_045962.2:n.1579G>A
|
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