ENST00000270357.10:c.1601A>G
MANE Select
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ENSP00000270357.4:p.Glu534Gly
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ENST00000270357.8:c.908A>G
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ENSP00000270357.3:p.Glu303Gly
|
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ENST00000437406.1:c.167A>G
|
ENSP00000403319.1:p.Glu56Gly
|
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ENST00000451363.5:c.242A>G
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ENSP00000414661.1:p.Glu81Gly
|
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ENST00000464550.5:n.437A>G
|
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ENST00000471657.1:n.404A>G
|
|
|
ENST00000481757.5:n.2535A>G
|
|
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ENST00000486058.5:n.1714A>G
|
|
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ENST00000493398.5:n.747A>G
|
|
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NM_018226.4:c.1601A>G
|
NP_060696.4:p.Glu534Gly
|
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XM_005247036.3:c.1568A>G
|
XP_005247093.1:p.Glu523Gly
|
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NM_018226.5:c.1601A>G
|
NP_060696.4:p.Glu534Gly
|
|
XM_005247036.4:c.1568A>G
|
XP_005247093.1:p.Glu523Gly
|
|
NM_018226.6:c.1601A>G
MANE Select
|
NP_060696.4:p.Glu534Gly
|
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