ENST00000220616.9:c.8142C>T
MANE Select
|
ENSP00000220616.4:p.Asp2714=
|
|
ENST00000220616.8:c.8142C>T
|
ENSP00000220616.4:p.Asp2714=
|
|
ENST00000519178.5:c.3508C>T
|
|
|
ENST00000519543.5:c.2541C>T
|
ENSP00000430430.1:p.Asp847=
|
|
ENST00000521107.1:c.354C>T
|
ENSP00000430161.1:p.Asp118=
|
|
ENST00000522691.1:n.228C>T
|
|
|
ENST00000523756.5:c.4797C>T
|
|
|
NM_003235.4:c.8142C>T
|
NP_003226.4:p.Asp2714=
|
|
XM_005251038.3:c.7950C>T
|
XP_005251095.1:p.Asp2650=
|
|
XM_006716622.2:c.8079C>T
|
XP_006716685.1:p.Asp2693=
|
|
XM_005251038.4:c.7950C>T
|
XP_005251095.1:p.Asp2650=
|
|
XM_006716622.3:c.8079C>T
|
XP_006716685.1:p.Asp2693=
|
|
XM_017013793.1:c.8076C>T
|
XP_016869282.1:p.Asp2692=
|
|
XM_017013794.1:c.8007C>T
|
XP_016869283.1:p.Asp2669=
|
|
XM_017013795.1:c.7971C>T
|
XP_016869284.1:p.Asp2657=
|
|
XM_017013796.1:c.7923C>T
|
XP_016869285.1:p.Asp2641=
|
|
XM_017013797.1:c.7881C>T
|
XP_016869286.1:p.Asp2627=
|
|
NM_003235.5:c.8142C>T
MANE Select
|
NP_003226.4:p.Asp2714=
|
|