ENST00000220616.9:c.8174T>G
MANE Select
|
ENSP00000220616.4:p.Leu2725Arg
|
|
ENST00000220616.8:c.8174T>G
|
ENSP00000220616.4:p.Leu2725Arg
|
|
ENST00000519178.5:c.3540T>G
|
|
|
ENST00000519543.5:c.2573T>G
|
ENSP00000430430.1:p.Leu858Arg
|
|
ENST00000521107.1:c.386T>G
|
ENSP00000430161.1:p.Leu129Arg
|
|
ENST00000522691.1:n.260T>G
|
|
|
ENST00000523756.5:c.4829T>G
|
|
|
NM_003235.4:c.8174T>G
|
NP_003226.4:p.Leu2725Arg
|
|
XM_005251038.3:c.7982T>G
|
XP_005251095.1:p.Leu2661Arg
|
|
XM_006716622.2:c.8111T>G
|
XP_006716685.1:p.Leu2704Arg
|
|
XM_005251038.4:c.7982T>G
|
XP_005251095.1:p.Leu2661Arg
|
|
XM_006716622.3:c.8111T>G
|
XP_006716685.1:p.Leu2704Arg
|
|
XM_017013793.1:c.8108T>G
|
XP_016869282.1:p.Leu2703Arg
|
|
XM_017013794.1:c.8039T>G
|
XP_016869283.1:p.Leu2680Arg
|
|
XM_017013795.1:c.8003T>G
|
XP_016869284.1:p.Leu2668Arg
|
|
XM_017013796.1:c.7955T>G
|
XP_016869285.1:p.Leu2652Arg
|
|
XM_017013797.1:c.7913T>G
|
XP_016869286.1:p.Leu2638Arg
|
|
NM_003235.5:c.8174T>G
MANE Select
|
NP_003226.4:p.Leu2725Arg
|
|