ENST00000682153.1:c.*1603A>G
(VPS13B)
|
ENSP00000507923.1:n.*1603A>G
|
|
ENST00000682358.1:n.12579A>G
(VPS13B)
|
|
|
ENST00000683334.1:c.*7631A>G
(VPS13B)
|
ENSP00000507369.1:n.*7631A>G
|
|
ENST00000357162.7:c.11874A>G
(VPS13B)
MANE Select
|
ENSP00000349685.2:p.Ala3958=
|
|
ENST00000358544.7:c.11949A>G
(VPS13B)
MANE Plus Clinical
|
ENSP00000351346.2:p.Ala3983=
|
|
ENST00000357162.6:c.11874A>G
(VPS13B)
|
ENSP00000349685.2:p.Ala3958=
|
|
ENST00000358544.6:c.11949A>G
(VPS13B)
|
ENSP00000351346.2:p.Ala3983=
|
|
ENST00000493587.1:n.1451A>G
(VPS13B)
|
|
|
ENST00000520517.5:c.*142-454T>C
(COX6C)
|
ENSP00000429991.1:n.*142-454T>C
|
|
ENST00000522934.5:c.*142-2253T>C
(COX6C)
|
ENSP00000428702.1:n.*142-2253T>C
|
|
NM_017890.4:c.11949A>G , LRG_351t1:c.11949A>G
(VPS13B)
|
NP_060360.3:p.Ala3983=
|
|
NM_152564.4:c.11874A>G , LRG_351t2:c.11874A>G
(VPS13B)
|
NP_689777.3:p.Ala3958=
|
|
XM_005250800.2:c.11949A>G
(VPS13B)
|
XP_005250857.1:p.Ala3983=
|
|
XM_005250801.3:c.11949A>G
(VPS13B)
|
XP_005250858.1:p.Ala3983=
|
|
XM_011516848.1:c.11946A>G
(VPS13B)
|
XP_011515150.1:p.Ala3982=
|
|
XM_011516849.1:c.11871A>G
(VPS13B)
|
XP_011515151.1:p.Ala3957=
|
|
XM_011516850.1:c.11571A>G
(VPS13B)
|
XP_011515152.1:p.Ala3857=
|
|
XM_011516851.1:c.8835A>G
(VPS13B)
|
XP_011515153.1:p.Ala2945=
|
|
XM_011516852.1:c.8835A>G
(VPS13B)
|
XP_011515154.1:p.Ala2945=
|
|
XM_011516854.1:c.7728A>G
(VPS13B)
|
XP_011515156.1:p.Ala2576=
|
|
XM_005250800.3:c.11949A>G
(VPS13B)
|
XP_005250857.1:p.Ala3983=
|
|
XM_005250801.5:c.11949A>G
(VPS13B)
|
XP_005250858.1:p.Ala3983=
|
|
XM_011516848.2:c.11946A>G
(VPS13B)
|
XP_011515150.1:p.Ala3982=
|
|
XM_011516849.2:c.11871A>G
(VPS13B)
|
XP_011515151.1:p.Ala3957=
|
|
XM_011516850.2:c.11571A>G
(VPS13B)
|
XP_011515152.1:p.Ala3857=
|
|
XM_011516851.2:c.8835A>G
(VPS13B)
|
XP_011515153.1:p.Ala2945=
|
|
XM_011516852.2:c.8835A>G
(VPS13B)
|
XP_011515154.1:p.Ala2945=
|
|
XM_011516854.2:c.7728A>G
(VPS13B)
|
XP_011515156.1:p.Ala2576=
|
|
XM_017013109.1:c.11754A>G
(VPS13B)
|
XP_016868598.1:p.Ala3918=
|
|
XM_017013111.1:c.8835A>G
(VPS13B)
|
XP_016868600.1:p.Ala2945=
|
|
XM_017013112.1:c.7506A>G
(VPS13B)
|
XP_016868601.1:p.Ala2502=
|
|
XM_024447074.1:c.10734A>G
(VPS13B)
|
XP_024302842.1:p.Ala3578=
|
|
NM_017890.5:c.11949A>G
(VPS13B)
MANE Plus Clinical
|
NP_060360.3:p.Ala3983=
|
|
NM_152564.5:c.11874A>G
(VPS13B)
MANE Select
|
NP_689777.3:p.Ala3958=
|
|