ENST00000682153.1:c.*1562A>C
(VPS13B)
|
ENSP00000507923.1:n.*1562A>C
|
|
ENST00000682358.1:n.12538A>C
(VPS13B)
|
|
|
ENST00000683334.1:c.*7590A>C
(VPS13B)
|
ENSP00000507369.1:n.*7590A>C
|
|
ENST00000357162.7:c.11833A>C
(VPS13B)
MANE Select
|
ENSP00000349685.2:p.Ser3945Arg
|
|
ENST00000358544.7:c.11908A>C
(VPS13B)
MANE Plus Clinical
|
ENSP00000351346.2:p.Ser3970Arg
|
|
ENST00000357162.6:c.11833A>C
(VPS13B)
|
ENSP00000349685.2:p.Ser3945Arg
|
|
ENST00000358544.6:c.11908A>C
(VPS13B)
|
ENSP00000351346.2:p.Ser3970Arg
|
|
ENST00000493587.1:n.1410A>C
(VPS13B)
|
|
|
ENST00000520517.5:c.*142-413T>G
(COX6C)
|
ENSP00000429991.1:n.*142-413T>G
|
|
ENST00000522934.5:c.*142-2212T>G
(COX6C)
|
ENSP00000428702.1:n.*142-2212T>G
|
|
NM_017890.4:c.11908A>C , LRG_351t1:c.11908A>C
(VPS13B)
|
NP_060360.3:p.Ser3970Arg
|
|
NM_152564.4:c.11833A>C , LRG_351t2:c.11833A>C
(VPS13B)
|
NP_689777.3:p.Ser3945Arg
|
|
XM_005250800.2:c.11908A>C
(VPS13B)
|
XP_005250857.1:p.Ser3970Arg
|
|
XM_005250801.3:c.11908A>C
(VPS13B)
|
XP_005250858.1:p.Ser3970Arg
|
|
XM_011516848.1:c.11905A>C
(VPS13B)
|
XP_011515150.1:p.Ser3969Arg
|
|
XM_011516849.1:c.11830A>C
(VPS13B)
|
XP_011515151.1:p.Ser3944Arg
|
|
XM_011516850.1:c.11530A>C
(VPS13B)
|
XP_011515152.1:p.Ser3844Arg
|
|
XM_011516851.1:c.8794A>C
(VPS13B)
|
XP_011515153.1:p.Ser2932Arg
|
|
XM_011516852.1:c.8794A>C
(VPS13B)
|
XP_011515154.1:p.Ser2932Arg
|
|
XM_011516854.1:c.7687A>C
(VPS13B)
|
XP_011515156.1:p.Ser2563Arg
|
|
XM_005250800.3:c.11908A>C
(VPS13B)
|
XP_005250857.1:p.Ser3970Arg
|
|
XM_005250801.5:c.11908A>C
(VPS13B)
|
XP_005250858.1:p.Ser3970Arg
|
|
XM_011516848.2:c.11905A>C
(VPS13B)
|
XP_011515150.1:p.Ser3969Arg
|
|
XM_011516849.2:c.11830A>C
(VPS13B)
|
XP_011515151.1:p.Ser3944Arg
|
|
XM_011516850.2:c.11530A>C
(VPS13B)
|
XP_011515152.1:p.Ser3844Arg
|
|
XM_011516851.2:c.8794A>C
(VPS13B)
|
XP_011515153.1:p.Ser2932Arg
|
|
XM_011516852.2:c.8794A>C
(VPS13B)
|
XP_011515154.1:p.Ser2932Arg
|
|
XM_011516854.2:c.7687A>C
(VPS13B)
|
XP_011515156.1:p.Ser2563Arg
|
|
XM_017013109.1:c.11713A>C
(VPS13B)
|
XP_016868598.1:p.Ser3905Arg
|
|
XM_017013111.1:c.8794A>C
(VPS13B)
|
XP_016868600.1:p.Ser2932Arg
|
|
XM_017013112.1:c.7465A>C
(VPS13B)
|
XP_016868601.1:p.Ser2489Arg
|
|
XM_024447074.1:c.10693A>C
(VPS13B)
|
XP_024302842.1:p.Ser3565Arg
|
|
NM_017890.5:c.11908A>C
(VPS13B)
MANE Plus Clinical
|
NP_060360.3:p.Ser3970Arg
|
|
NM_152564.5:c.11833A>C
(VPS13B)
MANE Select
|
NP_689777.3:p.Ser3945Arg
|
|