ENST00000220616.9:c.8022C>T
MANE Select
|
ENSP00000220616.4:p.Phe2674=
|
|
ENST00000220616.8:c.8022C>T
|
ENSP00000220616.4:p.Phe2674=
|
|
ENST00000519178.5:c.3388C>T
|
|
|
ENST00000519543.5:c.2421C>T
|
ENSP00000430430.1:p.Phe807=
|
|
ENST00000521107.1:c.234C>T
|
ENSP00000430161.1:p.Phe78=
|
|
ENST00000522691.1:n.108C>T
|
|
|
ENST00000523756.5:c.4677C>T
|
|
|
NM_003235.4:c.8022C>T
|
NP_003226.4:p.Phe2674=
|
|
XM_005251038.3:c.7830C>T
|
XP_005251095.1:p.Phe2610=
|
|
XM_006716622.2:c.7959C>T
|
XP_006716685.1:p.Phe2653=
|
|
XM_005251038.4:c.7830C>T
|
XP_005251095.1:p.Phe2610=
|
|
XM_006716622.3:c.7959C>T
|
XP_006716685.1:p.Phe2653=
|
|
XM_017013793.1:c.7956C>T
|
XP_016869282.1:p.Phe2652=
|
|
XM_017013794.1:c.7887C>T
|
XP_016869283.1:p.Phe2629=
|
|
XM_017013795.1:c.7851C>T
|
XP_016869284.1:p.Phe2617=
|
|
XM_017013796.1:c.7803C>T
|
XP_016869285.1:p.Phe2601=
|
|
XM_017013797.1:c.7761C>T
|
XP_016869286.1:p.Phe2587=
|
|
NM_003235.5:c.8022C>T
MANE Select
|
NP_003226.4:p.Phe2674=
|
|