ENST00000482750.6:c.706C>G
|
ENSP00000421262.2:p.His236Asp
|
|
ENST00000696903.1:n.757C>G
|
|
|
ENST00000374202.7:c.706C>G
MANE Select
|
ENSP00000363318.3:p.His236Asp
|
|
ENST00000642473.1:n.1070C>G
|
|
|
ENST00000644022.1:n.972C>G
|
|
|
ENST00000644708.1:n.1112C>G
|
|
|
ENST00000644911.1:n.1112C>G
|
|
|
ENST00000645266.1:c.706C>G
|
ENSP00000493734.1:p.His236Asp
|
|
ENST00000645518.1:c.706C>G
|
ENSP00000493986.1:p.His236Asp
|
|
ENST00000646106.1:c.706C>G
|
ENSP00000496437.1:p.His236Asp
|
|
ENST00000646505.1:c.706C>G
|
ENSP00000496673.1:p.His236Asp
|
|
ENST00000647492.1:c.706C>G
|
ENSP00000495340.1:p.His236Asp
|
|
ENST00000276110.6:n.1299C>G
|
|
|
ENST00000374188.7:c.-11C>G
|
ENSP00000363303.3:n.-11C>G
|
|
ENST00000374202.6:c.706C>G
|
ENSP00000363318.2:p.His236Asp
|
|
ENST00000456850.6:c.136C>G
|
ENSP00000388967.2:p.His46Asp
|
|
ENST00000464642.5:c.574C>G
|
ENSP00000425233.1:p.His192Asp
|
|
ENST00000482750.5:c.119C>G
|
|
|
ENST00000512747.3:n.633C>G
|
|
|
NM_000206.2:c.706C>G , LRG_150t1:c.706C>G
|
NP_000197.1:p.His236Asp
|
|
NM_000206.3:c.706C>G
MANE Select
|
NP_000197.1:p.His236Asp
|
|