ENST00000685553.1:c.*705C>T
|
ENSP00000510193.1:n.*705C>T
|
|
ENST00000687496.1:c.684C>T
|
ENSP00000509551.1:p.Asp228=
|
|
ENST00000688598.1:c.684C>T
|
ENSP00000510410.1:p.Asp228=
|
|
ENST00000691812.1:c.786C>T
|
ENSP00000510211.1:p.Asp262=
|
|
ENST00000693759.1:c.*398C>T
|
ENSP00000509518.1:n.*398C>T
|
|
ENST00000370803.8:c.786C>T
MANE Select
|
ENSP00000359839.4:p.Asp262=
|
|
ENST00000332070.7:c.786C>T
|
ENSP00000329097.3:p.Asp262=
|
|
ENST00000370799.5:c.789C>T
|
ENSP00000359835.1:p.Asp263=
|
|
ENST00000370800.4:c.789C>T
|
ENSP00000359836.4:p.Asp263=
|
|
ENST00000370803.7:c.786C>T
|
ENSP00000359839.3:p.Asp262=
|
|
ENST00000625464.2:c.789C>T
|
ENSP00000487420.1:p.Asp263=
|
|
NM_001015877.1:c.786C>T , LRG_629t1:c.786C>T
|
NP_001015877.1:p.Asp262=
|
|
NM_032335.3:c.789C>T , LRG_629t2:c.789C>T
|
NP_115711.2:p.Asp263=
|
|
NM_032458.2:c.786C>T
|
NP_115834.1:p.Asp262=
|
|
NM_001015877.2:c.786C>T
MANE Select
|
NP_001015877.1:p.Asp262=
|
|
NM_032458.3:c.786C>T
|
NP_115834.1:p.Asp262=
|
|