ENST00000220616.9:c.8109G>T
MANE Select
|
ENSP00000220616.4:p.Leu2703=
|
|
ENST00000220616.8:c.8109G>T
|
ENSP00000220616.4:p.Leu2703=
|
|
ENST00000519178.5:c.3475G>T
|
|
|
ENST00000519543.5:c.2508G>T
|
ENSP00000430430.1:p.Leu836=
|
|
ENST00000521107.1:c.321G>T
|
ENSP00000430161.1:p.Leu107=
|
|
ENST00000522691.1:n.195G>T
|
|
|
ENST00000523756.5:c.4764G>T
|
|
|
NM_003235.4:c.8109G>T
|
NP_003226.4:p.Leu2703=
|
|
XM_005251038.3:c.7917G>T
|
XP_005251095.1:p.Leu2639=
|
|
XM_006716622.2:c.8046G>T
|
XP_006716685.1:p.Leu2682=
|
|
XM_005251038.4:c.7917G>T
|
XP_005251095.1:p.Leu2639=
|
|
XM_006716622.3:c.8046G>T
|
XP_006716685.1:p.Leu2682=
|
|
XM_017013793.1:c.8043G>T
|
XP_016869282.1:p.Leu2681=
|
|
XM_017013794.1:c.7974G>T
|
XP_016869283.1:p.Leu2658=
|
|
XM_017013795.1:c.7938G>T
|
XP_016869284.1:p.Leu2646=
|
|
XM_017013796.1:c.7890G>T
|
XP_016869285.1:p.Leu2630=
|
|
XM_017013797.1:c.7848G>T
|
XP_016869286.1:p.Leu2616=
|
|
NM_003235.5:c.8109G>T
MANE Select
|
NP_003226.4:p.Leu2703=
|
|