ENST00000269980.7:c.755T>G
MANE Select
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ENSP00000269980.2:p.Phe252Cys
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ENST00000269980.6:c.755T>G
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ENSP00000269980.2:p.Phe252Cys
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ENST00000457836.6:c.689T>G
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ENSP00000416000.2:p.Phe230Cys
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ENST00000535632.5:n.384T>G
|
|
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ENST00000540732.3:c.857T>G
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ENSP00000443246.1:p.Phe286Cys
|
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ENST00000542943.5:c.668T>G
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ENSP00000440345.1:p.Phe223Cys
|
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ENST00000545787.1:n.383T>G
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|
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ENST00000595085.5:c.755T>G
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ENSP00000471150.2:p.Phe252Cys
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NM_000709.3:c.755T>G
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NP_000700.1:p.Phe252Cys
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NM_001164783.1:c.755T>G
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NP_001158255.1:p.Phe252Cys
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NM_000709.4:c.755T>G
MANE Select
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NP_000700.1:p.Phe252Cys
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NM_001164783.2:c.755T>G
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NP_001158255.1:p.Phe252Cys
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