ENST00000682275.1:c.505G=
|
ENSP00000507852.1:p.Glu169=
|
|
ENST00000683395.1:c.495G=
|
|
|
ENST00000684087.1:c.505G=
|
ENSP00000506978.1:p.Glu169=
|
|
ENST00000684700.1:c.505G=
|
ENSP00000507806.1:p.Glu169=
|
|
ENST00000506362.2:c.256G=
|
ENSP00000424103.2:p.Glu86=
|
|
ENST00000673642.1:c.304G=
|
ENSP00000501242.1:p.Glu102=
|
|
ENST00000673991.1:c.505G=
|
ENSP00000501033.1:p.Glu169=
|
|
ENST00000674051.1:c.379G=
|
ENSP00000501083.1:p.Glu127=
|
|
ENST00000226760.5:c.505G=
MANE Select
|
ENSP00000226760.1:p.Glu169=
|
|
ENST00000503569.5:c.505G=
|
ENSP00000423337.1:p.Glu169=
|
|
ENST00000506362.1:c.102G=
|
|
|
ENST00000507765.1:n.690G=
|
|
|
NM_001145853.1:c.505G=
|
NP_001139325.1:p.Glu169=
|
|
NM_006005.3:c.505G=
MANE Select
|
NP_005996.2:p.Glu169=
|
|
XM_017008586.1:c.514G=
|
XP_016864075.1:p.Glu172=
|
|