|
ENST00000682153.1:c.*428G>A
|
ENSP00000507923.1:n.*428G>A
|
|
|
ENST00000682358.1:n.11404G>A
|
|
|
|
ENST00000683334.1:c.*7016G>A
|
ENSP00000507369.1:n.*7016G>A
|
|
|
ENST00000357162.7:c.11259G>A
MANE Select
|
ENSP00000349685.2:p.Gln3753=
|
|
|
ENST00000358544.7:c.11334G>A
MANE Plus Clinical
|
ENSP00000351346.2:p.Gln3778=
|
|
|
ENST00000357162.6:c.11259G>A
|
ENSP00000349685.2:p.Gln3753=
|
|
|
ENST00000358544.6:c.11334G>A
|
ENSP00000351346.2:p.Gln3778=
|
|
|
ENST00000493587.1:n.276G>A
|
|
|
|
NM_017890.4:c.11334G>A , LRG_351t1:c.11334G>A
|
NP_060360.3:p.Gln3778=
|
|
|
NM_152564.4:c.11259G>A , LRG_351t2:c.11259G>A
|
NP_689777.3:p.Gln3753=
|
|
|
XM_005250800.2:c.11334G>A
|
XP_005250857.1:p.Gln3778=
|
|
|
XM_005250801.3:c.11334G>A
|
XP_005250858.1:p.Gln3778=
|
|
|
XM_011516848.1:c.11331G>A
|
XP_011515150.1:p.Gln3777=
|
|
|
XM_011516849.1:c.11256G>A
|
XP_011515151.1:p.Gln3752=
|
|
|
XM_011516850.1:c.10956G>A
|
XP_011515152.1:p.Gln3652=
|
|
|
XM_011516851.1:c.8220G>A
|
XP_011515153.1:p.Gln2740=
|
|
|
XM_011516852.1:c.8220G>A
|
XP_011515154.1:p.Gln2740=
|
|
|
XM_011516854.1:c.7113G>A
|
XP_011515156.1:p.Gln2371=
|
|
|
XM_005250800.3:c.11334G>A
|
XP_005250857.1:p.Gln3778=
|
|
|
XM_005250801.5:c.11334G>A
|
XP_005250858.1:p.Gln3778=
|
|
|
XM_011516848.2:c.11331G>A
|
XP_011515150.1:p.Gln3777=
|
|
|
XM_011516849.2:c.11256G>A
|
XP_011515151.1:p.Gln3752=
|
|
|
XM_011516850.2:c.10956G>A
|
XP_011515152.1:p.Gln3652=
|
|
|
XM_011516851.2:c.8220G>A
|
XP_011515153.1:p.Gln2740=
|
|
|
XM_011516852.2:c.8220G>A
|
XP_011515154.1:p.Gln2740=
|
|
|
XM_011516854.2:c.7113G>A
|
XP_011515156.1:p.Gln2371=
|
|
|
XM_017013109.1:c.11139G>A
|
XP_016868598.1:p.Gln3713=
|
|
|
XM_017013111.1:c.8220G>A
|
XP_016868600.1:p.Gln2740=
|
|
|
XM_017013112.1:c.6891G>A
|
XP_016868601.1:p.Gln2297=
|
|
|
XM_024447074.1:c.10119G>A
|
XP_024302842.1:p.Gln3373=
|
|
|
NM_017890.5:c.11334G>A
MANE Plus Clinical
|
NP_060360.3:p.Gln3778=
|
|
|
NM_152564.5:c.11259G>A
MANE Select
|
NP_689777.3:p.Gln3753=
|
|
