ENST00000698727.1:n.1252T>G
|
|
|
ENST00000698728.1:n.1771T>G
|
|
|
ENST00000698729.1:n.3317T>G
|
|
|
ENST00000698730.1:n.3317T>G
|
|
|
ENST00000698731.1:c.2051T>G
|
ENSP00000513898.1:p.Leu684Arg
|
|
ENST00000698732.1:c.*1053T>G
|
ENSP00000513899.1:n.*1053T>G
|
|
ENST00000698733.1:c.*1379T>G
|
ENSP00000513900.1:n.*1379T>G
|
|
ENST00000698734.1:c.2192T>G
|
ENSP00000513901.1:p.Leu731Arg
|
|
ENST00000698735.1:n.2307T>G
|
|
|
ENST00000698736.1:n.2307T>G
|
|
|
ENST00000698737.1:n.2307T>G
|
|
|
ENST00000698738.1:n.2307T>G
|
|
|
ENST00000698739.1:n.2307T>G
|
|
|
ENST00000372371.8:c.2192T>G
MANE Select
|
ENSP00000361446.3:p.Leu731Arg
|
|
ENST00000372371.7:c.2192T>G
|
ENSP00000361446.3:p.Leu731Arg
|
|
ENST00000472014.5:n.414T>G
|
|
|
ENST00000473588.2:c.855T>G
|
|
|
NM_007055.3:c.2192T>G
|
NP_008986.2:p.Leu731Arg
|
|
NM_007055.4:c.2192T>G
MANE Select
|
NP_008986.2:p.Leu731Arg
|
|