|
ENST00000371068.11:c.972T>G
MANE Select
|
ENSP00000360107.4:p.Tyr324Ter
|
|
|
ENST00000480623.6:c.972T>G
|
ENSP00000434498.2:p.Tyr324Ter
|
|
|
ENST00000635760.1:c.648T>G
|
ENSP00000489765.1:p.Tyr216Ter
|
|
|
ENST00000635812.1:c.*273T>G
|
ENSP00000490859.1:n.*273T>G
|
|
|
ENST00000635866.1:c.*841T>G
|
ENSP00000489866.1:n.*841T>G
|
|
|
ENST00000635911.1:n.2490T>G
|
|
|
|
ENST00000635984.1:c.648T>G
|
ENSP00000489921.1:p.Tyr216Ter
|
|
|
ENST00000635996.1:c.972T>G
|
ENSP00000490256.1:p.Tyr324Ter
|
|
|
ENST00000636107.1:c.972T>G
|
ENSP00000489680.1:p.Tyr324Ter
|
|
|
ENST00000636311.1:n.866T>G
|
|
|
|
ENST00000636343.1:c.638T>G
|
|
|
|
ENST00000636379.1:c.684T>G
|
ENSP00000490622.1:p.Tyr228Ter
|
|
|
ENST00000636398.1:c.672T>G
|
ENSP00000489654.1:n.672T>G
|
|
|
ENST00000636489.1:c.915T>G
|
ENSP00000489998.1:p.Tyr305Ter
|
|
|
ENST00000636616.1:n.588T>G
|
|
|
|
ENST00000636702.1:c.942T>G
|
ENSP00000489623.1:p.Tyr314Ter
|
|
|
ENST00000636954.1:c.915T>G
|
ENSP00000489966.1:p.Tyr305Ter
|
|
|
ENST00000637089.1:c.972T>G
|
ENSP00000489854.1:p.Tyr324Ter
|
|
|
ENST00000637263.1:c.972T>G
|
ENSP00000489700.1:p.Tyr324Ter
|
|
|
ENST00000637340.1:n.2897T>G
|
|
|
|
ENST00000637353.1:c.972T>G
|
ENSP00000490441.1:p.Tyr324Ter
|
|
|
ENST00000637602.1:c.*673T>G
|
ENSP00000490074.1:n.*673T>G
|
|
|
ENST00000637849.1:n.1036T>G
|
|
|
|
ENST00000637874.1:c.83-4383T>G
|
ENSP00000490348.1:n.83-4383T>G
|
|
|
ENST00000637892.1:n.1176T>G
|
|
|
|
ENST00000371068.9:c.972T>G
|
ENSP00000360107.4:p.Tyr324Ter
|
|
|
ENST00000480623.5:c.*1392T>G
|
ENSP00000434498.1:n.*1392T>G
|
|
|
ENST00000538167.2:c.915T>G
|
ENSP00000444521.1:p.Tyr305Ter
|
|
|
NM_001172420.1:c.915T>G
|
NP_001165891.1:p.Tyr305Ter
|
|
|
NM_018100.3:c.972T>G
|
NP_060570.2:p.Tyr324Ter
|
|
|
NR_033327.1:n.2444T>G
|
|
|
|
NM_018100.4:c.972T>G
MANE Select
|
NP_060570.2:p.Tyr324Ter
|
|
|
NM_001172420.2:c.915T>G
|
NP_001165891.1:p.Tyr305Ter
|
|
|
NR_033327.2:n.2298T>G
|
|
|
