ENST00000682114.1:c.121T>C
|
ENSP00000507245.1:p.Tyr41His
|
|
ENST00000682478.1:n.97T>C
|
|
|
ENST00000683576.1:n.97T>C
|
|
|
ENST00000683627.1:c.121T>C
|
ENSP00000507533.1:p.Tyr41His
|
|
ENST00000684082.1:c.121T>C
|
ENSP00000508266.1:p.Tyr41His
|
|
ENST00000684633.1:n.93T>C
|
|
|
ENST00000684678.1:c.117T>C
|
ENSP00000507059.1:p.Ser39=
|
|
ENST00000369842.9:c.121T>C
MANE Select
|
ENSP00000358857.4:p.Tyr41His
|
|
ENST00000369835.3:c.82+162T>C
|
ENSP00000358850.3:n.82+162T>C
|
|
ENST00000369842.8:c.121T>C
|
ENSP00000358857.4:p.Tyr41His
|
|
ENST00000428228.5:c.*26T>C
|
ENSP00000401081.1:n.*26T>C
|
|
ENST00000468294.5:n.81T>C
|
|
|
ENST00000485261.1:n.163+162T>C
|
|
|
ENST00000486738.5:n.265T>C
|
|
|
ENST00000492448.1:n.104T>C
|
|
|
ENST00000494443.5:n.178T>C
|
|
|
NM_000117.2:c.121T>C , LRG_745t1:c.121T>C
|
NP_000108.1:p.Tyr41His
|
|
XM_024452349.1:c.-88T>C
|
XP_024308117.1:n.-88T>C
|
|
NM_000117.3:c.121T>C
MANE Select
|
NP_000108.1:p.Tyr41His
|
|