ENST00000389857.11:c.5196C>A
MANE Select
|
ENSP00000374507.6:p.Thr1732=
|
|
ENST00000331194.8:c.768C>A
|
ENSP00000330332.8:p.Thr256=
|
|
ENST00000334448.5:n.1008C>A
|
|
|
ENST00000389857.10:c.5196C>A
|
ENSP00000374507.6:p.Thr1732=
|
|
ENST00000556726.5:c.1424C>A
|
|
|
NM_001080414.3:c.5196C>A
|
NP_001073883.2:p.Thr1732=
|
|
XM_011536796.1:c.5088C>A
|
XP_011535098.1:p.Thr1696=
|
|
XR_429316.2:n.5471C>A
|
|
|
XM_011536796.2:c.5088C>A
|
XP_011535098.1:p.Thr1696=
|
|
XM_017021336.1:c.2277C>A
|
XP_016876825.1:p.Thr759=
|
|
XR_429316.4:n.5469C>A
|
|
|
NM_001080414.4:c.5196C>A
MANE Select
|
NP_001073883.2:p.Thr1732=
|
|