ENST00000220616.9:c.6726C>A
MANE Select
|
ENSP00000220616.4:p.Arg2242=
|
|
ENST00000220616.8:c.6726C>A
|
ENSP00000220616.4:p.Arg2242=
|
|
ENST00000518108.1:c.168+75C>A
|
|
|
ENST00000519178.5:c.2092C>A
|
|
|
ENST00000519543.5:c.1125C>A
|
ENSP00000430430.1:p.Arg375=
|
|
ENST00000522523.5:n.787C>A
|
|
|
ENST00000523756.5:c.3381C>A
|
|
|
NM_003235.4:c.6726C>A
|
NP_003226.4:p.Arg2242=
|
|
XM_005251038.3:c.6534C>A
|
XP_005251095.1:p.Arg2178=
|
|
XM_006716622.2:c.6663C>A
|
XP_006716685.1:p.Arg2221=
|
|
XM_005251038.4:c.6534C>A
|
XP_005251095.1:p.Arg2178=
|
|
XM_006716622.3:c.6663C>A
|
XP_006716685.1:p.Arg2221=
|
|
XM_017013793.1:c.6660C>A
|
XP_016869282.1:p.Arg2220=
|
|
XM_017013794.1:c.6726C>A
|
XP_016869283.1:p.Arg2242=
|
|
XM_017013795.1:c.6555C>A
|
XP_016869284.1:p.Arg2185=
|
|
XM_017013796.1:c.6507C>A
|
XP_016869285.1:p.Arg2169=
|
|
XM_017013797.1:c.6465C>A
|
XP_016869286.1:p.Arg2155=
|
|
XM_017013798.1:c.6726C>A
|
XP_016869287.1:p.Arg2242=
|
|
NM_003235.5:c.6726C>A
MANE Select
|
NP_003226.4:p.Arg2242=
|
|