ENST00000220616.9:c.8104G=
MANE Select
|
ENSP00000220616.4:p.Glu2702=
|
|
ENST00000220616.8:c.8104G=
|
ENSP00000220616.4:p.Glu2702=
|
|
ENST00000519178.5:c.3470G=
|
|
|
ENST00000519543.5:c.2503G=
|
ENSP00000430430.1:p.Glu835=
|
|
ENST00000521107.1:c.316G=
|
ENSP00000430161.1:p.Glu106=
|
|
ENST00000522691.1:n.190G=
|
|
|
ENST00000523756.5:c.4759G=
|
|
|
NM_003235.4:c.8104G=
|
NP_003226.4:p.Glu2702=
|
|
XM_005251038.3:c.7912G=
|
XP_005251095.1:p.Glu2638=
|
|
XM_006716622.2:c.8041G=
|
XP_006716685.1:p.Glu2681=
|
|
XM_005251038.4:c.7912G=
|
XP_005251095.1:p.Glu2638=
|
|
XM_006716622.3:c.8041G=
|
XP_006716685.1:p.Glu2681=
|
|
XM_017013793.1:c.8038G=
|
XP_016869282.1:p.Glu2680=
|
|
XM_017013794.1:c.7969G=
|
XP_016869283.1:p.Glu2657=
|
|
XM_017013795.1:c.7933G=
|
XP_016869284.1:p.Glu2645=
|
|
XM_017013796.1:c.7885G=
|
XP_016869285.1:p.Glu2629=
|
|
XM_017013797.1:c.7843G=
|
XP_016869286.1:p.Glu2615=
|
|
NM_003235.5:c.8104G=
MANE Select
|
NP_003226.4:p.Glu2702=
|
|