ENST00000269321.12:c.445T>C
MANE Select
|
ENSP00000269321.7:p.Tyr149His
|
|
ENST00000269321.11:c.445T>C
|
ENSP00000269321.7:p.Tyr149His
|
|
ENST00000400721.8:c.416-103T>C
|
ENSP00000383556.4:n.416-103T>C
|
|
ENST00000541078.6:c.445T>C
|
ENSP00000441348.2:p.Tyr149His
|
|
ENST00000579121.5:c.445T>C
|
ENSP00000462960.1:p.Tyr149His
|
|
ENST00000580033.5:c.*89T>C
|
ENSP00000463530.1:n.*89T>C
|
|
ENST00000580685.5:c.445T>C
|
ENSP00000464205.1:p.Tyr149His
|
|
ENST00000581876.5:c.220T>C
|
ENSP00000461956.1:p.Tyr74His
|
|
ENST00000582984.5:n.647T>C
|
|
|
ENST00000583791.1:n.309T>C
|
|
|
ENST00000583868.5:c.435+10T>C
|
ENSP00000462209.1:n.435+10T>C
|
|
ENST00000584461.5:c.445T>C
|
ENSP00000463939.1:p.Tyr149His
|
|
NM_001185077.2:c.445T>C
|
NP_001172006.1:p.Tyr149His
|
|
NM_001185078.2:c.416-103T>C
|
NP_001172007.1:n.416-103T>C
|
|
NM_001301240.1:c.445T>C
|
NP_001288169.1:p.Tyr149His
|
|
NM_001301241.1:c.445T>C
|
NP_001288170.1:p.Tyr149His
|
|
NM_001301242.1:c.435+10T>C
|
NP_001288171.1:n.435+10T>C
|
|
NM_001301243.1:c.580T>C
|
NP_001288172.1:p.Tyr194His
|
|
NM_004309.5:c.445T>C
|
NP_004300.1:p.Tyr149His
|
|
NR_125441.1:n.504T>C
|
|
|
XM_011523574.1:c.580T>C
|
XP_011521876.1:p.Tyr194His
|
|
NM_004309.6:c.445T>C
MANE Select
|
NP_004300.1:p.Tyr149His
|
|
NM_001185077.3:c.445T>C
|
NP_001172006.1:p.Tyr149His
|
|
NM_001185078.3:c.416-103T>C
|
NP_001172007.1:n.416-103T>C
|
|
NM_001301240.2:c.445T>C
|
NP_001288169.1:p.Tyr149His
|
|
NM_001301241.2:c.445T>C
|
NP_001288170.1:p.Tyr149His
|
|
NM_001301242.2:c.435+10T>C
|
NP_001288171.1:n.435+10T>C
|
|
NM_001301243.2:c.580T>C
|
NP_001288172.1:p.Tyr194His
|
|
NR_125441.2:n.435T>C
|
|
|