ENST00000371068.11:c.949G>T
MANE Select
|
ENSP00000360107.4:p.Asp317Tyr
|
|
ENST00000480623.6:c.949G>T
|
ENSP00000434498.2:p.Asp317Tyr
|
|
ENST00000635760.1:c.625G>T
|
ENSP00000489765.1:p.Asp209Tyr
|
|
ENST00000635812.1:c.*250G>T
|
ENSP00000490859.1:n.*250G>T
|
|
ENST00000635866.1:c.*818G>T
|
ENSP00000489866.1:n.*818G>T
|
|
ENST00000635911.1:n.2467G>T
|
|
|
ENST00000635984.1:c.625G>T
|
ENSP00000489921.1:p.Asp209Tyr
|
|
ENST00000635996.1:c.949G>T
|
ENSP00000490256.1:p.Asp317Tyr
|
|
ENST00000636107.1:c.949G>T
|
ENSP00000489680.1:p.Asp317Tyr
|
|
ENST00000636311.1:n.843G>T
|
|
|
ENST00000636343.1:c.615G>T
|
|
|
ENST00000636379.1:c.661G>T
|
ENSP00000490622.1:p.Asp221Tyr
|
|
ENST00000636398.1:c.649G>T
|
ENSP00000489654.1:n.649G>T
|
|
ENST00000636489.1:c.892G>T
|
ENSP00000489998.1:p.Asp298Tyr
|
|
ENST00000636616.1:n.565G>T
|
|
|
ENST00000636702.1:c.919G>T
|
ENSP00000489623.1:p.Asp307Tyr
|
|
ENST00000636954.1:c.892G>T
|
ENSP00000489966.1:p.Asp298Tyr
|
|
ENST00000637089.1:c.949G>T
|
ENSP00000489854.1:p.Asp317Tyr
|
|
ENST00000637263.1:c.949G>T
|
ENSP00000489700.1:p.Asp317Tyr
|
|
ENST00000637340.1:n.2874G>T
|
|
|
ENST00000637353.1:c.949G>T
|
ENSP00000490441.1:p.Asp317Tyr
|
|
ENST00000637602.1:c.*650G>T
|
ENSP00000490074.1:n.*650G>T
|
|
ENST00000637849.1:n.1013G>T
|
|
|
ENST00000637874.1:c.83-4406G>T
|
ENSP00000490348.1:n.83-4406G>T
|
|
ENST00000637892.1:n.1153G>T
|
|
|
ENST00000371068.9:c.949G>T
|
ENSP00000360107.4:p.Asp317Tyr
|
|
ENST00000480623.5:c.*1369G>T
|
ENSP00000434498.1:n.*1369G>T
|
|
ENST00000538167.2:c.892G>T
|
ENSP00000444521.1:p.Asp298Tyr
|
|
NM_001172420.1:c.892G>T
|
NP_001165891.1:p.Asp298Tyr
|
|
NM_018100.3:c.949G>T
|
NP_060570.2:p.Asp317Tyr
|
|
NR_033327.1:n.2421G>T
|
|
|
NM_018100.4:c.949G>T
MANE Select
|
NP_060570.2:p.Asp317Tyr
|
|
NM_001172420.2:c.892G>T
|
NP_001165891.1:p.Asp298Tyr
|
|
NR_033327.2:n.2275G>T
|
|
|