ENST00000330062.8:c.635T>G
MANE Select
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ENSP00000331897.4:p.Phe212Cys
|
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ENST00000330062.7:c.635T>G
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ENSP00000331897.3:p.Phe212Cys
|
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ENST00000540499.2:c.479T>G
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ENSP00000446147.2:p.Phe160Cys
|
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ENST00000559482.5:c.308T>G
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ENSP00000453016.1:p.Phe103Cys
|
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ENST00000560061.1:c.*260T>G
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ENSP00000453254.1:n.*260T>G
|
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NM_001289910.1:c.479T>G , LRG_611t1:c.479T>G
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NP_001276839.1:p.Phe160Cys
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NM_001290114.1:c.245T>G
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NP_001277043.1:p.Phe82Cys
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NM_002168.3:c.635T>G , LRG_611t2:c.635T>G
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NP_002159.2:p.Phe212Cys
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NM_001290114.2:c.245T>G
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NP_001277043.1:p.Phe82Cys
|
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NM_002168.4:c.635T>G
MANE Select
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NP_002159.2:p.Phe212Cys
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