ENST00000309424.8:c.111T=
MANE Select
|
ENSP00000310966.3:p.Gly37=
|
|
ENST00000309424.7:c.111T=
|
ENSP00000310966.3:p.Gly37=
|
|
ENST00000589804.1:c.117T=
|
ENSP00000465099.1:p.Gly39=
|
|
ENST00000590794.1:c.20+464T=
|
|
|
ENST00000592852.1:c.-424T=
|
ENSP00000467771.1:n.-424T=
|
|
NM_001297590.1:c.117T=
|
NP_001284519.1:p.Gly39=
|
|
NM_012099.1:c.111T=
|
NP_036231.1:p.Gly37=
|
|
NM_001297590.2:c.117T=
|
NP_001284519.1:p.Gly39=
|
|
NM_012099.2:c.111T=
|
NP_036231.1:p.Gly37=
|
|
NM_001297590.3:c.117T=
|
NP_001284519.1:p.Gly39=
|
|
NM_012099.3:c.111T=
MANE Select
|
NP_036231.1:p.Gly37=
|
|