ENST00000682153.1:c.*1621T>A
(VPS13B)
|
ENSP00000507923.1:n.*1621T>A
|
|
ENST00000682358.1:n.12597T>A
(VPS13B)
|
|
|
ENST00000683334.1:c.*7649T>A
(VPS13B)
|
ENSP00000507369.1:n.*7649T>A
|
|
ENST00000357162.7:c.11892T>A
(VPS13B)
MANE Select
|
ENSP00000349685.2:p.Thr3964=
|
|
ENST00000358544.7:c.11967T>A
(VPS13B)
MANE Plus Clinical
|
ENSP00000351346.2:p.Thr3989=
|
|
ENST00000357162.6:c.11892T>A
(VPS13B)
|
ENSP00000349685.2:p.Thr3964=
|
|
ENST00000358544.6:c.11967T>A
(VPS13B)
|
ENSP00000351346.2:p.Thr3989=
|
|
ENST00000493587.1:n.1469T>A
(VPS13B)
|
|
|
ENST00000520517.5:c.*142-472A>T
(COX6C)
|
ENSP00000429991.1:n.*142-472A>T
|
|
ENST00000522934.5:c.*142-2271A>T
(COX6C)
|
ENSP00000428702.1:n.*142-2271A>T
|
|
NM_017890.4:c.11967T>A , LRG_351t1:c.11967T>A
(VPS13B)
|
NP_060360.3:p.Thr3989=
|
|
NM_152564.4:c.11892T>A , LRG_351t2:c.11892T>A
(VPS13B)
|
NP_689777.3:p.Thr3964=
|
|
XM_005250800.2:c.11967T>A
(VPS13B)
|
XP_005250857.1:p.Thr3989=
|
|
XM_005250801.3:c.11967T>A
(VPS13B)
|
XP_005250858.1:p.Thr3989=
|
|
XM_011516848.1:c.11964T>A
(VPS13B)
|
XP_011515150.1:p.Thr3988=
|
|
XM_011516849.1:c.11889T>A
(VPS13B)
|
XP_011515151.1:p.Thr3963=
|
|
XM_011516850.1:c.11589T>A
(VPS13B)
|
XP_011515152.1:p.Thr3863=
|
|
XM_011516851.1:c.8853T>A
(VPS13B)
|
XP_011515153.1:p.Thr2951=
|
|
XM_011516852.1:c.8853T>A
(VPS13B)
|
XP_011515154.1:p.Thr2951=
|
|
XM_011516854.1:c.7746T>A
(VPS13B)
|
XP_011515156.1:p.Thr2582=
|
|
XM_005250800.3:c.11967T>A
(VPS13B)
|
XP_005250857.1:p.Thr3989=
|
|
XM_005250801.5:c.11967T>A
(VPS13B)
|
XP_005250858.1:p.Thr3989=
|
|
XM_011516848.2:c.11964T>A
(VPS13B)
|
XP_011515150.1:p.Thr3988=
|
|
XM_011516849.2:c.11889T>A
(VPS13B)
|
XP_011515151.1:p.Thr3963=
|
|
XM_011516850.2:c.11589T>A
(VPS13B)
|
XP_011515152.1:p.Thr3863=
|
|
XM_011516851.2:c.8853T>A
(VPS13B)
|
XP_011515153.1:p.Thr2951=
|
|
XM_011516852.2:c.8853T>A
(VPS13B)
|
XP_011515154.1:p.Thr2951=
|
|
XM_011516854.2:c.7746T>A
(VPS13B)
|
XP_011515156.1:p.Thr2582=
|
|
XM_017013109.1:c.11772T>A
(VPS13B)
|
XP_016868598.1:p.Thr3924=
|
|
XM_017013111.1:c.8853T>A
(VPS13B)
|
XP_016868600.1:p.Thr2951=
|
|
XM_017013112.1:c.7524T>A
(VPS13B)
|
XP_016868601.1:p.Thr2508=
|
|
XM_024447074.1:c.10752T>A
(VPS13B)
|
XP_024302842.1:p.Thr3584=
|
|
NM_017890.5:c.11967T>A
(VPS13B)
MANE Plus Clinical
|
NP_060360.3:p.Thr3989=
|
|
NM_152564.5:c.11892T>A
(VPS13B)
MANE Select
|
NP_689777.3:p.Thr3964=
|
|