ENST00000220616.9:c.8129T>G
MANE Select
|
ENSP00000220616.4:p.Leu2710Arg
|
|
ENST00000220616.8:c.8129T>G
|
ENSP00000220616.4:p.Leu2710Arg
|
|
ENST00000519178.5:c.3495T>G
|
|
|
ENST00000519543.5:c.2528T>G
|
ENSP00000430430.1:p.Leu843Arg
|
|
ENST00000521107.1:c.341T>G
|
ENSP00000430161.1:p.Leu114Arg
|
|
ENST00000522691.1:n.215T>G
|
|
|
ENST00000523756.5:c.4784T>G
|
|
|
NM_003235.4:c.8129T>G
|
NP_003226.4:p.Leu2710Arg
|
|
XM_005251038.3:c.7937T>G
|
XP_005251095.1:p.Leu2646Arg
|
|
XM_006716622.2:c.8066T>G
|
XP_006716685.1:p.Leu2689Arg
|
|
XM_005251038.4:c.7937T>G
|
XP_005251095.1:p.Leu2646Arg
|
|
XM_006716622.3:c.8066T>G
|
XP_006716685.1:p.Leu2689Arg
|
|
XM_017013793.1:c.8063T>G
|
XP_016869282.1:p.Leu2688Arg
|
|
XM_017013794.1:c.7994T>G
|
XP_016869283.1:p.Leu2665Arg
|
|
XM_017013795.1:c.7958T>G
|
XP_016869284.1:p.Leu2653Arg
|
|
XM_017013796.1:c.7910T>G
|
XP_016869285.1:p.Leu2637Arg
|
|
XM_017013797.1:c.7868T>G
|
XP_016869286.1:p.Leu2623Arg
|
|
NM_003235.5:c.8129T>G
MANE Select
|
NP_003226.4:p.Leu2710Arg
|
|