ENST00000309755.9:c.1062G>A
MANE Select
|
ENSP00000312397.4:p.Gly354=
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|
ENST00000309755.8:c.1062G>A
|
ENSP00000312397.4:p.Gly354=
|
|
ENST00000502381.1:n.649G>A
|
|
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ENST00000504208.5:c.*335-10673G>A
|
ENSP00000423585.1:n.*335-10673G>A
|
|
ENST00000505853.1:c.942G>A
|
ENSP00000426173.1:p.Gly314=
|
|
ENST00000506491.5:c.816G>A
|
ENSP00000424828.1:p.Gly272=
|
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ENST00000506873.5:n.687G>A
|
|
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ENST00000508657.5:c.966G>A
|
ENSP00000422099.1:p.Gly322=
|
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NM_001257194.1:c.966G>A
|
NP_001244123.1:p.Gly322=
|
|
NM_001257195.1:c.816G>A
|
NP_001244124.1:p.Gly272=
|
|
NM_017415.2:c.1062G>A
|
NP_059111.2:p.Gly354=
|
|
NM_017415.3:c.1062G>A
MANE Select
|
NP_059111.2:p.Gly354=
|
|
NM_001257195.2:c.816G>A
|
NP_001244124.1:p.Gly272=
|
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