ENST00000220616.9:c.8042T>A
MANE Select
|
ENSP00000220616.4:p.Phe2681Tyr
|
|
ENST00000220616.8:c.8042T>A
|
ENSP00000220616.4:p.Phe2681Tyr
|
|
ENST00000519178.5:c.3408T>A
|
|
|
ENST00000519543.5:c.2441T>A
|
ENSP00000430430.1:p.Phe814Tyr
|
|
ENST00000521107.1:c.254T>A
|
ENSP00000430161.1:p.Phe85Tyr
|
|
ENST00000522691.1:n.128T>A
|
|
|
ENST00000523756.5:c.4697T>A
|
|
|
NM_003235.4:c.8042T>A
|
NP_003226.4:p.Phe2681Tyr
|
|
XM_005251038.3:c.7850T>A
|
XP_005251095.1:p.Phe2617Tyr
|
|
XM_006716622.2:c.7979T>A
|
XP_006716685.1:p.Phe2660Tyr
|
|
XM_005251038.4:c.7850T>A
|
XP_005251095.1:p.Phe2617Tyr
|
|
XM_006716622.3:c.7979T>A
|
XP_006716685.1:p.Phe2660Tyr
|
|
XM_017013793.1:c.7976T>A
|
XP_016869282.1:p.Phe2659Tyr
|
|
XM_017013794.1:c.7907T>A
|
XP_016869283.1:p.Phe2636Tyr
|
|
XM_017013795.1:c.7871T>A
|
XP_016869284.1:p.Phe2624Tyr
|
|
XM_017013796.1:c.7823T>A
|
XP_016869285.1:p.Phe2608Tyr
|
|
XM_017013797.1:c.7781T>A
|
XP_016869286.1:p.Phe2594Tyr
|
|
NM_003235.5:c.8042T>A
MANE Select
|
NP_003226.4:p.Phe2681Tyr
|
|