ENST00000682114.1:c.118G>A
|
ENSP00000507245.1:p.Glu40Lys
|
|
ENST00000682478.1:n.94G>A
|
|
|
ENST00000683576.1:n.94G>A
|
|
|
ENST00000683627.1:c.118G>A
|
ENSP00000507533.1:p.Glu40Lys
|
|
ENST00000684082.1:c.118G>A
|
ENSP00000508266.1:p.Glu40Lys
|
|
ENST00000684633.1:n.90G>A
|
|
|
ENST00000684678.1:c.114G>A
|
ENSP00000507059.1:p.Ser38=
|
|
ENST00000369842.9:c.118G>A
MANE Select
|
ENSP00000358857.4:p.Glu40Lys
|
|
ENST00000369835.3:c.82+159G>A
|
ENSP00000358850.3:n.82+159G>A
|
|
ENST00000369842.8:c.118G>A
|
ENSP00000358857.4:p.Glu40Lys
|
|
ENST00000428228.5:c.*23G>A
|
ENSP00000401081.1:n.*23G>A
|
|
ENST00000468294.5:n.78G>A
|
|
|
ENST00000485261.1:n.163+159G>A
|
|
|
ENST00000486738.5:n.262G>A
|
|
|
ENST00000492448.1:n.101G>A
|
|
|
ENST00000494443.5:n.175G>A
|
|
|
NM_000117.2:c.118G>A , LRG_745t1:c.118G>A
|
NP_000108.1:p.Glu40Lys
|
|
XM_024452349.1:c.-91G>A
|
XP_024308117.1:n.-91G>A
|
|
NM_000117.3:c.118G>A
MANE Select
|
NP_000108.1:p.Glu40Lys
|
|