ENST00000393078.5:c.872T>G
MANE Select
|
ENSP00000376793.3:p.Leu291Arg
|
|
ENST00000393078.4:c.872T>G
|
ENSP00000376793.3:p.Leu291Arg
|
|
ENST00000393080.8:c.872T>G
|
ENSP00000376795.4:p.Leu291Arg
|
|
ENST00000467132.5:c.872T>G
|
ENSP00000450540.1:p.Leu291Arg
|
|
ENST00000482740.2:c.218T>G
|
ENSP00000451119.1:p.Leu73Arg
|
|
ENST00000553947.1:c.1835T>G
|
|
|
ENST00000555820.1:c.872T>G
|
ENSP00000452246.3:p.Leu291Arg
|
|
ENST00000556388.1:n.58-2918T>G
|
|
|
ENST00000556968.2:c.644-2918T>G
|
ENSP00000452476.1:n.644-2918T>G
|
|
ENST00000621603.1:c.91T>G
|
|
|
NM_001085.4:c.872T>G
|
NP_001076.2:p.Leu291Arg
|
|
NM_001085.5:c.872T>G
MANE Select
|
NP_001076.2:p.Leu291Arg
|
|
NM_001384672.1:c.872T>G
|
NP_001371601.1:p.Leu291Arg
|
|
NM_001384673.1:c.872T>G
|
NP_001371602.1:p.Leu291Arg
|
|
NM_001384674.1:c.872T>G
|
NP_001371603.1:p.Leu291Arg
|
|