ENST00000270357.10:c.1602G>A
MANE Select
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ENSP00000270357.4:p.Glu534=
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ENST00000270357.8:c.909G>A
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ENSP00000270357.3:p.Glu303=
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ENST00000437406.1:c.168G>A
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ENSP00000403319.1:p.Glu56=
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ENST00000451363.5:c.243G>A
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ENSP00000414661.1:p.Glu81=
|
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ENST00000464550.5:n.438G>A
|
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ENST00000471657.1:n.405G>A
|
|
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ENST00000481757.5:n.2536G>A
|
|
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ENST00000486058.5:n.1715G>A
|
|
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ENST00000493398.5:n.748G>A
|
|
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NM_018226.4:c.1602G>A
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NP_060696.4:p.Glu534=
|
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XM_005247036.3:c.1569G>A
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XP_005247093.1:p.Glu523=
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NM_018226.5:c.1602G>A
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NP_060696.4:p.Glu534=
|
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XM_005247036.4:c.1569G>A
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XP_005247093.1:p.Glu523=
|
|
NM_018226.6:c.1602G>A
MANE Select
|
NP_060696.4:p.Glu534=
|
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