ENST00000682153.1:c.*1535A>T
(VPS13B)
|
ENSP00000507923.1:n.*1535A>T
|
|
ENST00000682358.1:n.12511A>T
(VPS13B)
|
|
|
ENST00000683334.1:c.*7563A>T
(VPS13B)
|
ENSP00000507369.1:n.*7563A>T
|
|
ENST00000357162.7:c.11806A>T
(VPS13B)
MANE Select
|
ENSP00000349685.2:p.Thr3936Ser
|
|
ENST00000358544.7:c.11881A>T
(VPS13B)
MANE Plus Clinical
|
ENSP00000351346.2:p.Thr3961Ser
|
|
ENST00000357162.6:c.11806A>T
(VPS13B)
|
ENSP00000349685.2:p.Thr3936Ser
|
|
ENST00000358544.6:c.11881A>T
(VPS13B)
|
ENSP00000351346.2:p.Thr3961Ser
|
|
ENST00000493587.1:n.1383A>T
(VPS13B)
|
|
|
ENST00000520517.5:c.*142-386T>A
(COX6C)
|
ENSP00000429991.1:n.*142-386T>A
|
|
ENST00000522934.5:c.*142-2185T>A
(COX6C)
|
ENSP00000428702.1:n.*142-2185T>A
|
|
NM_017890.4:c.11881A>T , LRG_351t1:c.11881A>T
(VPS13B)
|
NP_060360.3:p.Thr3961Ser
|
|
NM_152564.4:c.11806A>T , LRG_351t2:c.11806A>T
(VPS13B)
|
NP_689777.3:p.Thr3936Ser
|
|
XM_005250800.2:c.11881A>T
(VPS13B)
|
XP_005250857.1:p.Thr3961Ser
|
|
XM_005250801.3:c.11881A>T
(VPS13B)
|
XP_005250858.1:p.Thr3961Ser
|
|
XM_011516848.1:c.11878A>T
(VPS13B)
|
XP_011515150.1:p.Thr3960Ser
|
|
XM_011516849.1:c.11803A>T
(VPS13B)
|
XP_011515151.1:p.Thr3935Ser
|
|
XM_011516850.1:c.11503A>T
(VPS13B)
|
XP_011515152.1:p.Thr3835Ser
|
|
XM_011516851.1:c.8767A>T
(VPS13B)
|
XP_011515153.1:p.Thr2923Ser
|
|
XM_011516852.1:c.8767A>T
(VPS13B)
|
XP_011515154.1:p.Thr2923Ser
|
|
XM_011516854.1:c.7660A>T
(VPS13B)
|
XP_011515156.1:p.Thr2554Ser
|
|
XM_005250800.3:c.11881A>T
(VPS13B)
|
XP_005250857.1:p.Thr3961Ser
|
|
XM_005250801.5:c.11881A>T
(VPS13B)
|
XP_005250858.1:p.Thr3961Ser
|
|
XM_011516848.2:c.11878A>T
(VPS13B)
|
XP_011515150.1:p.Thr3960Ser
|
|
XM_011516849.2:c.11803A>T
(VPS13B)
|
XP_011515151.1:p.Thr3935Ser
|
|
XM_011516850.2:c.11503A>T
(VPS13B)
|
XP_011515152.1:p.Thr3835Ser
|
|
XM_011516851.2:c.8767A>T
(VPS13B)
|
XP_011515153.1:p.Thr2923Ser
|
|
XM_011516852.2:c.8767A>T
(VPS13B)
|
XP_011515154.1:p.Thr2923Ser
|
|
XM_011516854.2:c.7660A>T
(VPS13B)
|
XP_011515156.1:p.Thr2554Ser
|
|
XM_017013109.1:c.11686A>T
(VPS13B)
|
XP_016868598.1:p.Thr3896Ser
|
|
XM_017013111.1:c.8767A>T
(VPS13B)
|
XP_016868600.1:p.Thr2923Ser
|
|
XM_017013112.1:c.7438A>T
(VPS13B)
|
XP_016868601.1:p.Thr2480Ser
|
|
XM_024447074.1:c.10666A>T
(VPS13B)
|
XP_024302842.1:p.Thr3556Ser
|
|
NM_017890.5:c.11881A>T
(VPS13B)
MANE Plus Clinical
|
NP_060360.3:p.Thr3961Ser
|
|
NM_152564.5:c.11806A>T
(VPS13B)
MANE Select
|
NP_689777.3:p.Thr3936Ser
|
|