ENST00000220616.9:c.8071C>A
MANE Select
|
ENSP00000220616.4:p.Arg2691Ser
|
|
ENST00000220616.8:c.8071C>A
|
ENSP00000220616.4:p.Arg2691Ser
|
|
ENST00000519178.5:c.3437C>A
|
|
|
ENST00000519543.5:c.2470C>A
|
ENSP00000430430.1:p.Arg824Ser
|
|
ENST00000521107.1:c.283C>A
|
ENSP00000430161.1:p.Arg95Ser
|
|
ENST00000522691.1:n.157C>A
|
|
|
ENST00000523756.5:c.4726C>A
|
|
|
NM_003235.4:c.8071C>A
|
NP_003226.4:p.Arg2691Ser
|
|
XM_005251038.3:c.7879C>A
|
XP_005251095.1:p.Arg2627Ser
|
|
XM_006716622.2:c.8008C>A
|
XP_006716685.1:p.Arg2670Ser
|
|
XM_005251038.4:c.7879C>A
|
XP_005251095.1:p.Arg2627Ser
|
|
XM_006716622.3:c.8008C>A
|
XP_006716685.1:p.Arg2670Ser
|
|
XM_017013793.1:c.8005C>A
|
XP_016869282.1:p.Arg2669Ser
|
|
XM_017013794.1:c.7936C>A
|
XP_016869283.1:p.Arg2646Ser
|
|
XM_017013795.1:c.7900C>A
|
XP_016869284.1:p.Arg2634Ser
|
|
XM_017013796.1:c.7852C>A
|
XP_016869285.1:p.Arg2618Ser
|
|
XM_017013797.1:c.7810C>A
|
XP_016869286.1:p.Arg2604Ser
|
|
NM_003235.5:c.8071C>A
MANE Select
|
NP_003226.4:p.Arg2691Ser
|
|