ENST00000396705.10:c.652T>C
MANE Select
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ENSP00000379933.4:p.Cys218Arg
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ENST00000229270.8:c.763T>C
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ENSP00000229270.4:p.Cys255Arg
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ENST00000396705.9:c.652T>C
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ENSP00000379933.4:p.Cys218Arg
|
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ENST00000474253.1:n.141T>C
|
|
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ENST00000488464.6:c.406T>C
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ENSP00000475620.1:p.Cys136Arg
|
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ENST00000535434.5:c.406T>C
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ENSP00000443599.1:p.Cys136Arg
|
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ENST00000613953.4:c.763T>C
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ENSP00000484435.1:p.Cys255Arg
|
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NM_000365.5:c.652T>C
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NP_000356.1:p.Cys218Arg
|
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NM_001159287.1:c.763T>C
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NP_001152759.1:p.Cys255Arg
|
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NM_001258026.1:c.406T>C
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NP_001244955.1:p.Cys136Arg
|
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XR_002957378.1:n.1660T>C
|
|
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NM_000365.6:c.652T>C
MANE Select
|
NP_000356.1:p.Cys218Arg
|
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NM_001258026.2:c.406T>C
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NP_001244955.1:p.Cys136Arg
|
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