ENST00000392038.7:c.774G>A
MANE Select
|
ENSP00000375892.2:p.Glu258=
|
|
ENST00000578615.6:c.653G>A
|
|
|
ENST00000311278.10:c.774G>A
|
ENSP00000309428.6:p.Glu258=
|
|
ENST00000391844.8:c.*388G>A
|
ENSP00000375719.4:n.*388G>A
|
|
ENST00000391845.6:n.239G>A
|
|
|
ENST00000392038.6:c.774G>A
|
ENSP00000375892.2:p.Glu258=
|
|
ENST00000424901.5:c.774G>A
|
ENSP00000399532.2:p.Glu258=
|
|
ENST00000476266.5:n.1102G>A
|
|
|
ENST00000480878.6:n.201G>A
|
|
|
ENST00000483166.5:n.662G>A
|
|
|
ENST00000496089.6:n.41G>A
|
|
|
ENST00000578282.5:n.167G>A
|
|
|
ENST00000578310.1:c.75-1641G>A
|
|
|
ENST00000578615.5:c.342G>A
|
ENSP00000463262.1:p.Glu114=
|
|
ENST00000579047.5:c.588G>A
|
ENSP00000471369.1:p.Glu196=
|
|
ENST00000579345.5:n.294G>A
|
|
|
ENST00000580878.1:n.431G>A
|
|
|
ENST00000584288.5:c.*388G>A
|
ENSP00000462469.1:n.*388G>A
|
|
ENST00000601166.5:c.518G>A
|
ENSP00000472371.1:n.518G>A
|
|
NM_001243027.2:c.588G>A
|
NP_001229956.1:p.Glu196=
|
|
NM_001243028.2:c.588G>A
|
NP_001229957.1:p.Glu196=
|
|
NM_001626.5:c.774G>A
|
NP_001617.1:p.Glu258=
|
|
XM_011526614.1:c.774G>A
|
XP_011524916.1:p.Glu258=
|
|
XM_011526615.1:c.774G>A
|
XP_011524917.1:p.Glu258=
|
|
XM_011526616.1:c.774G>A
|
XP_011524918.1:p.Glu258=
|
|
XM_011526617.1:c.774G>A
|
XP_011524919.1:p.Glu258=
|
|
XM_011526618.1:c.774G>A
|
XP_011524920.1:p.Glu258=
|
|
XM_011526619.1:c.774G>A
|
XP_011524921.1:p.Glu258=
|
|
XM_011526620.1:c.774G>A
|
XP_011524922.1:p.Glu258=
|
|
XM_011526621.1:c.774G>A
|
XP_011524923.1:p.Glu258=
|
|
XM_011526622.1:c.774G>A
|
XP_011524924.1:p.Glu258=
|
|
NM_001330511.1:c.774G>A
|
NP_001317440.1:p.Glu258=
|
|
XM_011526622.2:c.774G>A
|
XP_011524924.1:p.Glu258=
|
|
XM_017026470.2:c.774G>A
|
XP_016881959.1:p.Glu258=
|
|
XM_024451416.1:c.774G>A
|
XP_024307184.1:p.Glu258=
|
|
XM_024451417.1:c.774G>A
|
XP_024307185.1:p.Glu258=
|
|
NM_001626.6:c.774G>A
MANE Select
|
NP_001617.1:p.Glu258=
|
|
NM_001243027.3:c.588G>A
|
NP_001229956.1:p.Glu196=
|
|
NM_001243028.3:c.588G>A
|
NP_001229957.1:p.Glu196=
|
|