ENST00000462619.6:n.550C>T
(TNFSF12)
|
|
|
ENST00000462811.2:n.271C>T
(TNFSF12)
|
|
|
ENST00000700014.1:c.*143C>T
(TNFSF12)
|
ENSP00000514755.1:n.*143C>T
|
|
ENST00000700015.1:c.436C>T
(TNFSF12)
|
ENSP00000514756.1:p.Arg146Cys
|
|
ENST00000700047.1:n.435C>T
(TNFSF12)
|
|
|
ENST00000700048.1:n.677C>T
(TNFSF12)
|
|
|
ENST00000700049.1:n.429C>T
(TNFSF12)
|
|
|
ENST00000700050.1:n.680C>T
(TNFSF12)
|
|
|
ENST00000700052.1:c.374-262C>T
(TNFSF12)
|
ENSP00000514764.1:n.374-262C>T
|
|
ENST00000700053.1:c.430C>T
(TNFSF12)
|
ENSP00000514765.1:p.Arg144Cys
|
|
ENST00000700054.1:c.*143C>T
(TNFSF12)
|
ENSP00000514766.1:n.*143C>T
|
|
ENST00000700056.1:c.*267C>T
(TNFSF12)
|
ENSP00000514767.1:n.*267C>T
|
|
ENST00000700057.1:n.521C>T
(TNFSF12)
|
|
|
ENST00000700058.1:n.535C>T
(TNFSF12)
|
|
|
ENST00000700059.1:n.802C>T
(TNFSF12)
|
|
|
ENST00000293825.11:c.433C>T
(TNFSF12)
MANE Select
|
ENSP00000293825.6:p.Arg145Cys
|
|
ENST00000293825.10:c.433C>T
(TNFSF12)
|
ENSP00000293825.6:p.Arg145Cys
|
|
ENST00000293826.4:c.433C>T
(TNFSF12-TNFSF13)
|
ENSP00000293826.4:p.Arg145Cys
|
|
ENST00000322272.11:c.*267C>T
(TNFSF12)
|
ENSP00000314636.7:n.*267C>T
|
|
ENST00000462619.5:n.323C>T
(TNFSF12)
|
|
|
ENST00000462811.1:n.264C>T
(TNFSF12)
|
|
|
NM_003809.2:c.433C>T
(TNFSF12)
|
NP_003800.1:p.Arg145Cys
|
|
NM_172089.3:c.433C>T
(TNFSF12-TNFSF13)
|
NP_742086.1:p.Arg145Cys
|
|
NR_037146.1:n.768C>T
(TNFSF12)
|
|
|
NM_003809.3:c.433C>T
(TNFSF12)
MANE Select
|
NP_003800.1:p.Arg145Cys
|
|
NM_172089.4:c.433C>T
(TNFSF12-TNFSF13)
|
NP_742086.1:p.Arg145Cys
|
|
NR_037146.2:n.768C>T
(TNFSF12)
|
|
|