ENST00000682153.1:c.*368G>T
|
ENSP00000507923.1:n.*368G>T
|
|
ENST00000682358.1:n.11344G>T
|
|
|
ENST00000683334.1:c.*6956G>T
|
ENSP00000507369.1:n.*6956G>T
|
|
ENST00000357162.7:c.11199G>T
MANE Select
|
ENSP00000349685.2:p.Leu3733=
|
|
ENST00000358544.7:c.11274G>T
MANE Plus Clinical
|
ENSP00000351346.2:p.Leu3758=
|
|
ENST00000357162.6:c.11199G>T
|
ENSP00000349685.2:p.Leu3733=
|
|
ENST00000358544.6:c.11274G>T
|
ENSP00000351346.2:p.Leu3758=
|
|
NM_017890.4:c.11274G>T , LRG_351t1:c.11274G>T
|
NP_060360.3:p.Leu3758=
|
|
NM_152564.4:c.11199G>T , LRG_351t2:c.11199G>T
|
NP_689777.3:p.Leu3733=
|
|
XM_005250800.2:c.11274G>T
|
XP_005250857.1:p.Leu3758=
|
|
XM_005250801.3:c.11274G>T
|
XP_005250858.1:p.Leu3758=
|
|
XM_011516848.1:c.11271G>T
|
XP_011515150.1:p.Leu3757=
|
|
XM_011516849.1:c.11196G>T
|
XP_011515151.1:p.Leu3732=
|
|
XM_011516850.1:c.10896G>T
|
XP_011515152.1:p.Leu3632=
|
|
XM_011516851.1:c.8160G>T
|
XP_011515153.1:p.Leu2720=
|
|
XM_011516852.1:c.8160G>T
|
XP_011515154.1:p.Leu2720=
|
|
XM_011516854.1:c.7053G>T
|
XP_011515156.1:p.Leu2351=
|
|
XM_005250800.3:c.11274G>T
|
XP_005250857.1:p.Leu3758=
|
|
XM_005250801.5:c.11274G>T
|
XP_005250858.1:p.Leu3758=
|
|
XM_011516848.2:c.11271G>T
|
XP_011515150.1:p.Leu3757=
|
|
XM_011516849.2:c.11196G>T
|
XP_011515151.1:p.Leu3732=
|
|
XM_011516850.2:c.10896G>T
|
XP_011515152.1:p.Leu3632=
|
|
XM_011516851.2:c.8160G>T
|
XP_011515153.1:p.Leu2720=
|
|
XM_011516852.2:c.8160G>T
|
XP_011515154.1:p.Leu2720=
|
|
XM_011516854.2:c.7053G>T
|
XP_011515156.1:p.Leu2351=
|
|
XM_017013109.1:c.11079G>T
|
XP_016868598.1:p.Leu3693=
|
|
XM_017013111.1:c.8160G>T
|
XP_016868600.1:p.Leu2720=
|
|
XM_017013112.1:c.6831G>T
|
XP_016868601.1:p.Leu2277=
|
|
XM_024447074.1:c.10059G>T
|
XP_024302842.1:p.Leu3353=
|
|
NM_017890.5:c.11274G>T
MANE Plus Clinical
|
NP_060360.3:p.Leu3758=
|
|
NM_152564.5:c.11199G>T
MANE Select
|
NP_689777.3:p.Leu3733=
|
|