ENST00000370646.9:c.597T>C
MANE Select
|
ENSP00000359680.4:p.Gly199=
|
|
ENST00000370642.4:c.7T>C
|
|
|
ENST00000370646.8:c.597T>C
|
ENSP00000359680.4:p.Gly199=
|
|
ENST00000370647.8:c.212-2049T>C
|
ENSP00000359681.4:n.212-2049T>C
|
|
ENST00000370649.3:c.212-2049T>C
|
ENSP00000359683.3:n.212-2049T>C
|
|
ENST00000465608.1:n.1441T>C
|
|
|
NM_001134670.1:c.212-2049T>C
|
NP_001128142.1:n.212-2049T>C
|
|
NM_138413.3:c.597T>C
|
NP_612422.2:p.Gly199=
|
|
NM_138413.4:c.597T>C
MANE Select
|
NP_612422.2:p.Gly199=
|
|
NM_001134670.2:c.212-2049T>C
|
NP_001128142.1:n.212-2049T>C
|
|