ENST00000682153.1:c.*1570T>C
(VPS13B)
|
ENSP00000507923.1:n.*1570T>C
|
|
ENST00000682358.1:n.12546T>C
(VPS13B)
|
|
|
ENST00000683334.1:c.*7598T>C
(VPS13B)
|
ENSP00000507369.1:n.*7598T>C
|
|
ENST00000357162.7:c.11841T>C
(VPS13B)
MANE Select
|
ENSP00000349685.2:p.Ser3947=
|
|
ENST00000358544.7:c.11916T>C
(VPS13B)
MANE Plus Clinical
|
ENSP00000351346.2:p.Ser3972=
|
|
ENST00000357162.6:c.11841T>C
(VPS13B)
|
ENSP00000349685.2:p.Ser3947=
|
|
ENST00000358544.6:c.11916T>C
(VPS13B)
|
ENSP00000351346.2:p.Ser3972=
|
|
ENST00000493587.1:n.1418T>C
(VPS13B)
|
|
|
ENST00000520517.5:c.*142-421A>G
(COX6C)
|
ENSP00000429991.1:n.*142-421A>G
|
|
ENST00000522934.5:c.*142-2220A>G
(COX6C)
|
ENSP00000428702.1:n.*142-2220A>G
|
|
NM_017890.4:c.11916T>C , LRG_351t1:c.11916T>C
(VPS13B)
|
NP_060360.3:p.Ser3972=
|
|
NM_152564.4:c.11841T>C , LRG_351t2:c.11841T>C
(VPS13B)
|
NP_689777.3:p.Ser3947=
|
|
XM_005250800.2:c.11916T>C
(VPS13B)
|
XP_005250857.1:p.Ser3972=
|
|
XM_005250801.3:c.11916T>C
(VPS13B)
|
XP_005250858.1:p.Ser3972=
|
|
XM_011516848.1:c.11913T>C
(VPS13B)
|
XP_011515150.1:p.Ser3971=
|
|
XM_011516849.1:c.11838T>C
(VPS13B)
|
XP_011515151.1:p.Ser3946=
|
|
XM_011516850.1:c.11538T>C
(VPS13B)
|
XP_011515152.1:p.Ser3846=
|
|
XM_011516851.1:c.8802T>C
(VPS13B)
|
XP_011515153.1:p.Ser2934=
|
|
XM_011516852.1:c.8802T>C
(VPS13B)
|
XP_011515154.1:p.Ser2934=
|
|
XM_011516854.1:c.7695T>C
(VPS13B)
|
XP_011515156.1:p.Ser2565=
|
|
XM_005250800.3:c.11916T>C
(VPS13B)
|
XP_005250857.1:p.Ser3972=
|
|
XM_005250801.5:c.11916T>C
(VPS13B)
|
XP_005250858.1:p.Ser3972=
|
|
XM_011516848.2:c.11913T>C
(VPS13B)
|
XP_011515150.1:p.Ser3971=
|
|
XM_011516849.2:c.11838T>C
(VPS13B)
|
XP_011515151.1:p.Ser3946=
|
|
XM_011516850.2:c.11538T>C
(VPS13B)
|
XP_011515152.1:p.Ser3846=
|
|
XM_011516851.2:c.8802T>C
(VPS13B)
|
XP_011515153.1:p.Ser2934=
|
|
XM_011516852.2:c.8802T>C
(VPS13B)
|
XP_011515154.1:p.Ser2934=
|
|
XM_011516854.2:c.7695T>C
(VPS13B)
|
XP_011515156.1:p.Ser2565=
|
|
XM_017013109.1:c.11721T>C
(VPS13B)
|
XP_016868598.1:p.Ser3907=
|
|
XM_017013111.1:c.8802T>C
(VPS13B)
|
XP_016868600.1:p.Ser2934=
|
|
XM_017013112.1:c.7473T>C
(VPS13B)
|
XP_016868601.1:p.Ser2491=
|
|
XM_024447074.1:c.10701T>C
(VPS13B)
|
XP_024302842.1:p.Ser3567=
|
|
NM_017890.5:c.11916T>C
(VPS13B)
MANE Plus Clinical
|
NP_060360.3:p.Ser3972=
|
|
NM_152564.5:c.11841T>C
(VPS13B)
MANE Select
|
NP_689777.3:p.Ser3947=
|
|