ENST00000220616.9:c.8111T>G
MANE Select
|
ENSP00000220616.4:p.Leu2704Arg
|
|
ENST00000220616.8:c.8111T>G
|
ENSP00000220616.4:p.Leu2704Arg
|
|
ENST00000519178.5:c.3477T>G
|
|
|
ENST00000519543.5:c.2510T>G
|
ENSP00000430430.1:p.Leu837Arg
|
|
ENST00000521107.1:c.323T>G
|
ENSP00000430161.1:p.Leu108Arg
|
|
ENST00000522691.1:n.197T>G
|
|
|
ENST00000523756.5:c.4766T>G
|
|
|
NM_003235.4:c.8111T>G
|
NP_003226.4:p.Leu2704Arg
|
|
XM_005251038.3:c.7919T>G
|
XP_005251095.1:p.Leu2640Arg
|
|
XM_006716622.2:c.8048T>G
|
XP_006716685.1:p.Leu2683Arg
|
|
XM_005251038.4:c.7919T>G
|
XP_005251095.1:p.Leu2640Arg
|
|
XM_006716622.3:c.8048T>G
|
XP_006716685.1:p.Leu2683Arg
|
|
XM_017013793.1:c.8045T>G
|
XP_016869282.1:p.Leu2682Arg
|
|
XM_017013794.1:c.7976T>G
|
XP_016869283.1:p.Leu2659Arg
|
|
XM_017013795.1:c.7940T>G
|
XP_016869284.1:p.Leu2647Arg
|
|
XM_017013796.1:c.7892T>G
|
XP_016869285.1:p.Leu2631Arg
|
|
XM_017013797.1:c.7850T>G
|
XP_016869286.1:p.Leu2617Arg
|
|
NM_003235.5:c.8111T>G
MANE Select
|
NP_003226.4:p.Leu2704Arg
|
|