ENST00000682114.1:c.239A=
|
ENSP00000507245.1:p.Glu80=
|
|
ENST00000682478.1:n.215A=
|
|
|
ENST00000683576.1:n.215A=
|
|
|
ENST00000683627.1:c.239A=
|
ENSP00000507533.1:p.Glu80=
|
|
ENST00000684082.1:c.239A=
|
ENSP00000508266.1:p.Glu80=
|
|
ENST00000684633.1:n.211A=
|
|
|
ENST00000684678.1:c.235A=
|
ENSP00000507059.1:n.235A=
|
|
ENST00000369842.9:c.239A=
MANE Select
|
ENSP00000358857.4:p.Glu80=
|
|
ENST00000369835.3:c.134A=
|
ENSP00000358850.3:p.Glu45=
|
|
ENST00000369842.8:c.239A=
|
ENSP00000358857.4:p.Glu80=
|
|
ENST00000428228.5:c.*144A=
|
ENSP00000401081.1:n.*144A=
|
|
ENST00000468294.5:n.199A=
|
|
|
ENST00000485261.1:n.215A=
|
|
|
ENST00000486738.5:n.383A=
|
|
|
ENST00000492448.1:n.222A=
|
|
|
ENST00000494443.5:n.296A=
|
|
|
NM_000117.2:c.239A= , LRG_745t1:c.239A=
|
NP_000108.1:p.Glu80=
|
|
XM_024452349.1:c.31A=
|
XP_024308117.1:p.Arg11=
|
|
NM_000117.3:c.239A=
MANE Select
|
NP_000108.1:p.Glu80=
|
|