ENST00000220616.9:c.8149T>A
MANE Select
|
ENSP00000220616.4:p.Phe2717Ile
|
|
ENST00000220616.8:c.8149T>A
|
ENSP00000220616.4:p.Phe2717Ile
|
|
ENST00000519178.5:c.3515T>A
|
|
|
ENST00000519543.5:c.2548T>A
|
ENSP00000430430.1:p.Phe850Ile
|
|
ENST00000521107.1:c.361T>A
|
ENSP00000430161.1:p.Phe121Ile
|
|
ENST00000522691.1:n.235T>A
|
|
|
ENST00000523756.5:c.4804T>A
|
|
|
NM_003235.4:c.8149T>A
|
NP_003226.4:p.Phe2717Ile
|
|
XM_005251038.3:c.7957T>A
|
XP_005251095.1:p.Phe2653Ile
|
|
XM_006716622.2:c.8086T>A
|
XP_006716685.1:p.Phe2696Ile
|
|
XM_005251038.4:c.7957T>A
|
XP_005251095.1:p.Phe2653Ile
|
|
XM_006716622.3:c.8086T>A
|
XP_006716685.1:p.Phe2696Ile
|
|
XM_017013793.1:c.8083T>A
|
XP_016869282.1:p.Phe2695Ile
|
|
XM_017013794.1:c.8014T>A
|
XP_016869283.1:p.Phe2672Ile
|
|
XM_017013795.1:c.7978T>A
|
XP_016869284.1:p.Phe2660Ile
|
|
XM_017013796.1:c.7930T>A
|
XP_016869285.1:p.Phe2644Ile
|
|
XM_017013797.1:c.7888T>A
|
XP_016869286.1:p.Phe2630Ile
|
|
NM_003235.5:c.8149T>A
MANE Select
|
NP_003226.4:p.Phe2717Ile
|
|