ENST00000682153.1:c.*1582A>G
(VPS13B)
|
ENSP00000507923.1:n.*1582A>G
|
|
ENST00000682358.1:n.12558A>G
(VPS13B)
|
|
|
ENST00000683334.1:c.*7610A>G
(VPS13B)
|
ENSP00000507369.1:n.*7610A>G
|
|
ENST00000357162.7:c.11853A>G
(VPS13B)
MANE Select
|
ENSP00000349685.2:p.Ile3951Met
|
|
ENST00000358544.7:c.11928A>G
(VPS13B)
MANE Plus Clinical
|
ENSP00000351346.2:p.Ile3976Met
|
|
ENST00000357162.6:c.11853A>G
(VPS13B)
|
ENSP00000349685.2:p.Ile3951Met
|
|
ENST00000358544.6:c.11928A>G
(VPS13B)
|
ENSP00000351346.2:p.Ile3976Met
|
|
ENST00000493587.1:n.1430A>G
(VPS13B)
|
|
|
ENST00000520517.5:c.*142-433T>C
(COX6C)
|
ENSP00000429991.1:n.*142-433T>C
|
|
ENST00000522934.5:c.*142-2232T>C
(COX6C)
|
ENSP00000428702.1:n.*142-2232T>C
|
|
NM_017890.4:c.11928A>G , LRG_351t1:c.11928A>G
(VPS13B)
|
NP_060360.3:p.Ile3976Met
|
|
NM_152564.4:c.11853A>G , LRG_351t2:c.11853A>G
(VPS13B)
|
NP_689777.3:p.Ile3951Met
|
|
XM_005250800.2:c.11928A>G
(VPS13B)
|
XP_005250857.1:p.Ile3976Met
|
|
XM_005250801.3:c.11928A>G
(VPS13B)
|
XP_005250858.1:p.Ile3976Met
|
|
XM_011516848.1:c.11925A>G
(VPS13B)
|
XP_011515150.1:p.Ile3975Met
|
|
XM_011516849.1:c.11850A>G
(VPS13B)
|
XP_011515151.1:p.Ile3950Met
|
|
XM_011516850.1:c.11550A>G
(VPS13B)
|
XP_011515152.1:p.Ile3850Met
|
|
XM_011516851.1:c.8814A>G
(VPS13B)
|
XP_011515153.1:p.Ile2938Met
|
|
XM_011516852.1:c.8814A>G
(VPS13B)
|
XP_011515154.1:p.Ile2938Met
|
|
XM_011516854.1:c.7707A>G
(VPS13B)
|
XP_011515156.1:p.Ile2569Met
|
|
XM_005250800.3:c.11928A>G
(VPS13B)
|
XP_005250857.1:p.Ile3976Met
|
|
XM_005250801.5:c.11928A>G
(VPS13B)
|
XP_005250858.1:p.Ile3976Met
|
|
XM_011516848.2:c.11925A>G
(VPS13B)
|
XP_011515150.1:p.Ile3975Met
|
|
XM_011516849.2:c.11850A>G
(VPS13B)
|
XP_011515151.1:p.Ile3950Met
|
|
XM_011516850.2:c.11550A>G
(VPS13B)
|
XP_011515152.1:p.Ile3850Met
|
|
XM_011516851.2:c.8814A>G
(VPS13B)
|
XP_011515153.1:p.Ile2938Met
|
|
XM_011516852.2:c.8814A>G
(VPS13B)
|
XP_011515154.1:p.Ile2938Met
|
|
XM_011516854.2:c.7707A>G
(VPS13B)
|
XP_011515156.1:p.Ile2569Met
|
|
XM_017013109.1:c.11733A>G
(VPS13B)
|
XP_016868598.1:p.Ile3911Met
|
|
XM_017013111.1:c.8814A>G
(VPS13B)
|
XP_016868600.1:p.Ile2938Met
|
|
XM_017013112.1:c.7485A>G
(VPS13B)
|
XP_016868601.1:p.Ile2495Met
|
|
XM_024447074.1:c.10713A>G
(VPS13B)
|
XP_024302842.1:p.Ile3571Met
|
|
NM_017890.5:c.11928A>G
(VPS13B)
MANE Plus Clinical
|
NP_060360.3:p.Ile3976Met
|
|
NM_152564.5:c.11853A>G
(VPS13B)
MANE Select
|
NP_689777.3:p.Ile3951Met
|
|