ENST00000682153.1:c.*1511T>C
(VPS13B)
|
ENSP00000507923.1:n.*1511T>C
|
|
ENST00000682358.1:n.12487T>C
(VPS13B)
|
|
|
ENST00000683334.1:c.*7539T>C
(VPS13B)
|
ENSP00000507369.1:n.*7539T>C
|
|
ENST00000357162.7:c.11782T>C
(VPS13B)
MANE Select
|
ENSP00000349685.2:p.Tyr3928His
|
|
ENST00000358544.7:c.11857T>C
(VPS13B)
MANE Plus Clinical
|
ENSP00000351346.2:p.Tyr3953His
|
|
ENST00000357162.6:c.11782T>C
(VPS13B)
|
ENSP00000349685.2:p.Tyr3928His
|
|
ENST00000358544.6:c.11857T>C
(VPS13B)
|
ENSP00000351346.2:p.Tyr3953His
|
|
ENST00000493587.1:n.1359T>C
(VPS13B)
|
|
|
ENST00000520517.5:c.*142-362A>G
(COX6C)
|
ENSP00000429991.1:n.*142-362A>G
|
|
ENST00000522934.5:c.*142-2161A>G
(COX6C)
|
ENSP00000428702.1:n.*142-2161A>G
|
|
NM_017890.4:c.11857T>C , LRG_351t1:c.11857T>C
(VPS13B)
|
NP_060360.3:p.Tyr3953His
|
|
NM_152564.4:c.11782T>C , LRG_351t2:c.11782T>C
(VPS13B)
|
NP_689777.3:p.Tyr3928His
|
|
XM_005250800.2:c.11857T>C
(VPS13B)
|
XP_005250857.1:p.Tyr3953His
|
|
XM_005250801.3:c.11857T>C
(VPS13B)
|
XP_005250858.1:p.Tyr3953His
|
|
XM_011516848.1:c.11854T>C
(VPS13B)
|
XP_011515150.1:p.Tyr3952His
|
|
XM_011516849.1:c.11779T>C
(VPS13B)
|
XP_011515151.1:p.Tyr3927His
|
|
XM_011516850.1:c.11479T>C
(VPS13B)
|
XP_011515152.1:p.Tyr3827His
|
|
XM_011516851.1:c.8743T>C
(VPS13B)
|
XP_011515153.1:p.Tyr2915His
|
|
XM_011516852.1:c.8743T>C
(VPS13B)
|
XP_011515154.1:p.Tyr2915His
|
|
XM_011516854.1:c.7636T>C
(VPS13B)
|
XP_011515156.1:p.Tyr2546His
|
|
XM_005250800.3:c.11857T>C
(VPS13B)
|
XP_005250857.1:p.Tyr3953His
|
|
XM_005250801.5:c.11857T>C
(VPS13B)
|
XP_005250858.1:p.Tyr3953His
|
|
XM_011516848.2:c.11854T>C
(VPS13B)
|
XP_011515150.1:p.Tyr3952His
|
|
XM_011516849.2:c.11779T>C
(VPS13B)
|
XP_011515151.1:p.Tyr3927His
|
|
XM_011516850.2:c.11479T>C
(VPS13B)
|
XP_011515152.1:p.Tyr3827His
|
|
XM_011516851.2:c.8743T>C
(VPS13B)
|
XP_011515153.1:p.Tyr2915His
|
|
XM_011516852.2:c.8743T>C
(VPS13B)
|
XP_011515154.1:p.Tyr2915His
|
|
XM_011516854.2:c.7636T>C
(VPS13B)
|
XP_011515156.1:p.Tyr2546His
|
|
XM_017013109.1:c.11662T>C
(VPS13B)
|
XP_016868598.1:p.Tyr3888His
|
|
XM_017013111.1:c.8743T>C
(VPS13B)
|
XP_016868600.1:p.Tyr2915His
|
|
XM_017013112.1:c.7414T>C
(VPS13B)
|
XP_016868601.1:p.Tyr2472His
|
|
XM_024447074.1:c.10642T>C
(VPS13B)
|
XP_024302842.1:p.Tyr3548His
|
|
NM_017890.5:c.11857T>C
(VPS13B)
MANE Plus Clinical
|
NP_060360.3:p.Tyr3953His
|
|
NM_152564.5:c.11782T>C
(VPS13B)
MANE Select
|
NP_689777.3:p.Tyr3928His
|
|