ENST00000270357.10:c.1591C>G
MANE Select
|
ENSP00000270357.4:p.Arg531Gly
|
|
ENST00000270357.8:c.898C>G
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ENSP00000270357.3:p.Arg300Gly
|
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ENST00000437406.1:c.157C>G
|
ENSP00000403319.1:p.Arg53Gly
|
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ENST00000451363.5:c.232C>G
|
ENSP00000414661.1:p.Arg78Gly
|
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ENST00000464550.5:n.427C>G
|
|
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ENST00000471657.1:n.394C>G
|
|
|
ENST00000481757.5:n.2525C>G
|
|
|
ENST00000486058.5:n.1704C>G
|
|
|
ENST00000493398.5:n.737C>G
|
|
|
NM_018226.4:c.1591C>G
|
NP_060696.4:p.Arg531Gly
|
|
XM_005247036.3:c.1558C>G
|
XP_005247093.1:p.Arg520Gly
|
|
NM_018226.5:c.1591C>G
|
NP_060696.4:p.Arg531Gly
|
|
XM_005247036.4:c.1558C>G
|
XP_005247093.1:p.Arg520Gly
|
|
NM_018226.6:c.1591C>G
MANE Select
|
NP_060696.4:p.Arg531Gly
|
|