ENST00000270357.10:c.1592G=
MANE Select
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ENSP00000270357.4:p.Arg531=
|
|
ENST00000270357.8:c.899G=
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ENSP00000270357.3:p.Arg300=
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|
ENST00000437406.1:c.158G=
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ENSP00000403319.1:p.Arg53=
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|
ENST00000451363.5:c.233G=
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ENSP00000414661.1:p.Arg78=
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ENST00000464550.5:n.428G=
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|
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ENST00000471657.1:n.395G=
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|
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ENST00000481757.5:n.2526G=
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|
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ENST00000486058.5:n.1705G=
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|
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ENST00000493398.5:n.738G=
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|
|
NM_018226.4:c.1592G=
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NP_060696.4:p.Arg531=
|
|
XM_005247036.3:c.1559G=
|
XP_005247093.1:p.Arg520=
|
|
NM_018226.5:c.1592G=
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NP_060696.4:p.Arg531=
|
|
XM_005247036.4:c.1559G=
|
XP_005247093.1:p.Arg520=
|
|
NM_018226.6:c.1592G=
MANE Select
|
NP_060696.4:p.Arg531=
|
|