ENST00000270357.10:c.1586T>G
MANE Select
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ENSP00000270357.4:p.Leu529Arg
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ENST00000270357.8:c.893T>G
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ENSP00000270357.3:p.Leu298Arg
|
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ENST00000437406.1:c.152T>G
|
ENSP00000403319.1:p.Leu51Arg
|
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ENST00000451363.5:c.227T>G
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ENSP00000414661.1:p.Leu76Arg
|
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ENST00000464550.5:n.422T>G
|
|
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ENST00000471657.1:n.389T>G
|
|
|
ENST00000481757.5:n.2520T>G
|
|
|
ENST00000486058.5:n.1699T>G
|
|
|
ENST00000493398.5:n.732T>G
|
|
|
NM_018226.4:c.1586T>G
|
NP_060696.4:p.Leu529Arg
|
|
XM_005247036.3:c.1553T>G
|
XP_005247093.1:p.Leu518Arg
|
|
NM_018226.5:c.1586T>G
|
NP_060696.4:p.Leu529Arg
|
|
XM_005247036.4:c.1553T>G
|
XP_005247093.1:p.Leu518Arg
|
|
NM_018226.6:c.1586T>G
MANE Select
|
NP_060696.4:p.Leu529Arg
|
|