ENST00000682153.1:c.*1527A>T
(VPS13B)
|
ENSP00000507923.1:n.*1527A>T
|
|
ENST00000682358.1:n.12503A>T
(VPS13B)
|
|
|
ENST00000683334.1:c.*7555A>T
(VPS13B)
|
ENSP00000507369.1:n.*7555A>T
|
|
ENST00000357162.7:c.11798A>T
(VPS13B)
MANE Select
|
ENSP00000349685.2:p.Asp3933Val
|
|
ENST00000358544.7:c.11873A>T
(VPS13B)
MANE Plus Clinical
|
ENSP00000351346.2:p.Asp3958Val
|
|
ENST00000357162.6:c.11798A>T
(VPS13B)
|
ENSP00000349685.2:p.Asp3933Val
|
|
ENST00000358544.6:c.11873A>T
(VPS13B)
|
ENSP00000351346.2:p.Asp3958Val
|
|
ENST00000493587.1:n.1375A>T
(VPS13B)
|
|
|
ENST00000520517.5:c.*142-378T>A
(COX6C)
|
ENSP00000429991.1:n.*142-378T>A
|
|
ENST00000522934.5:c.*142-2177T>A
(COX6C)
|
ENSP00000428702.1:n.*142-2177T>A
|
|
NM_017890.4:c.11873A>T , LRG_351t1:c.11873A>T
(VPS13B)
|
NP_060360.3:p.Asp3958Val
|
|
NM_152564.4:c.11798A>T , LRG_351t2:c.11798A>T
(VPS13B)
|
NP_689777.3:p.Asp3933Val
|
|
XM_005250800.2:c.11873A>T
(VPS13B)
|
XP_005250857.1:p.Asp3958Val
|
|
XM_005250801.3:c.11873A>T
(VPS13B)
|
XP_005250858.1:p.Asp3958Val
|
|
XM_011516848.1:c.11870A>T
(VPS13B)
|
XP_011515150.1:p.Asp3957Val
|
|
XM_011516849.1:c.11795A>T
(VPS13B)
|
XP_011515151.1:p.Asp3932Val
|
|
XM_011516850.1:c.11495A>T
(VPS13B)
|
XP_011515152.1:p.Asp3832Val
|
|
XM_011516851.1:c.8759A>T
(VPS13B)
|
XP_011515153.1:p.Asp2920Val
|
|
XM_011516852.1:c.8759A>T
(VPS13B)
|
XP_011515154.1:p.Asp2920Val
|
|
XM_011516854.1:c.7652A>T
(VPS13B)
|
XP_011515156.1:p.Asp2551Val
|
|
XM_005250800.3:c.11873A>T
(VPS13B)
|
XP_005250857.1:p.Asp3958Val
|
|
XM_005250801.5:c.11873A>T
(VPS13B)
|
XP_005250858.1:p.Asp3958Val
|
|
XM_011516848.2:c.11870A>T
(VPS13B)
|
XP_011515150.1:p.Asp3957Val
|
|
XM_011516849.2:c.11795A>T
(VPS13B)
|
XP_011515151.1:p.Asp3932Val
|
|
XM_011516850.2:c.11495A>T
(VPS13B)
|
XP_011515152.1:p.Asp3832Val
|
|
XM_011516851.2:c.8759A>T
(VPS13B)
|
XP_011515153.1:p.Asp2920Val
|
|
XM_011516852.2:c.8759A>T
(VPS13B)
|
XP_011515154.1:p.Asp2920Val
|
|
XM_011516854.2:c.7652A>T
(VPS13B)
|
XP_011515156.1:p.Asp2551Val
|
|
XM_017013109.1:c.11678A>T
(VPS13B)
|
XP_016868598.1:p.Asp3893Val
|
|
XM_017013111.1:c.8759A>T
(VPS13B)
|
XP_016868600.1:p.Asp2920Val
|
|
XM_017013112.1:c.7430A>T
(VPS13B)
|
XP_016868601.1:p.Asp2477Val
|
|
XM_024447074.1:c.10658A>T
(VPS13B)
|
XP_024302842.1:p.Asp3553Val
|
|
NM_017890.5:c.11873A>T
(VPS13B)
MANE Plus Clinical
|
NP_060360.3:p.Asp3958Val
|
|
NM_152564.5:c.11798A>T
(VPS13B)
MANE Select
|
NP_689777.3:p.Asp3933Val
|
|