|
ENST00000682153.1:c.*472G>A
|
ENSP00000507923.1:n.*472G>A
|
|
|
ENST00000682358.1:n.11448G>A
|
|
|
|
ENST00000683334.1:c.*7060G>A
|
ENSP00000507369.1:n.*7060G>A
|
|
|
ENST00000357162.7:c.11303G>A
MANE Select
|
ENSP00000349685.2:p.Gly3768Asp
|
|
|
ENST00000358544.7:c.11378G>A
MANE Plus Clinical
|
ENSP00000351346.2:p.Gly3793Asp
|
|
|
ENST00000357162.6:c.11303G>A
|
ENSP00000349685.2:p.Gly3768Asp
|
|
|
ENST00000358544.6:c.11378G>A
|
ENSP00000351346.2:p.Gly3793Asp
|
|
|
ENST00000493587.1:n.320G>A
|
|
|
|
NM_017890.4:c.11378G>A , LRG_351t1:c.11378G>A
|
NP_060360.3:p.Gly3793Asp
|
|
|
NM_152564.4:c.11303G>A , LRG_351t2:c.11303G>A
|
NP_689777.3:p.Gly3768Asp
|
|
|
XM_005250800.2:c.11378G>A
|
XP_005250857.1:p.Gly3793Asp
|
|
|
XM_005250801.3:c.11378G>A
|
XP_005250858.1:p.Gly3793Asp
|
|
|
XM_011516848.1:c.11375G>A
|
XP_011515150.1:p.Gly3792Asp
|
|
|
XM_011516849.1:c.11300G>A
|
XP_011515151.1:p.Gly3767Asp
|
|
|
XM_011516850.1:c.11000G>A
|
XP_011515152.1:p.Gly3667Asp
|
|
|
XM_011516851.1:c.8264G>A
|
XP_011515153.1:p.Gly2755Asp
|
|
|
XM_011516852.1:c.8264G>A
|
XP_011515154.1:p.Gly2755Asp
|
|
|
XM_011516854.1:c.7157G>A
|
XP_011515156.1:p.Gly2386Asp
|
|
|
XM_005250800.3:c.11378G>A
|
XP_005250857.1:p.Gly3793Asp
|
|
|
XM_005250801.5:c.11378G>A
|
XP_005250858.1:p.Gly3793Asp
|
|
|
XM_011516848.2:c.11375G>A
|
XP_011515150.1:p.Gly3792Asp
|
|
|
XM_011516849.2:c.11300G>A
|
XP_011515151.1:p.Gly3767Asp
|
|
|
XM_011516850.2:c.11000G>A
|
XP_011515152.1:p.Gly3667Asp
|
|
|
XM_011516851.2:c.8264G>A
|
XP_011515153.1:p.Gly2755Asp
|
|
|
XM_011516852.2:c.8264G>A
|
XP_011515154.1:p.Gly2755Asp
|
|
|
XM_011516854.2:c.7157G>A
|
XP_011515156.1:p.Gly2386Asp
|
|
|
XM_017013109.1:c.11183G>A
|
XP_016868598.1:p.Gly3728Asp
|
|
|
XM_017013111.1:c.8264G>A
|
XP_016868600.1:p.Gly2755Asp
|
|
|
XM_017013112.1:c.6935G>A
|
XP_016868601.1:p.Gly2312Asp
|
|
|
XM_024447074.1:c.10163G>A
|
XP_024302842.1:p.Gly3388Asp
|
|
|
NM_017890.5:c.11378G>A
MANE Plus Clinical
|
NP_060360.3:p.Gly3793Asp
|
|
|
NM_152564.5:c.11303G>A
MANE Select
|
NP_689777.3:p.Gly3768Asp
|
|
