ENST00000685553.1:c.*703G>C
|
ENSP00000510193.1:n.*703G>C
|
|
ENST00000687496.1:c.682G>C
|
ENSP00000509551.1:p.Asp228His
|
|
ENST00000688598.1:c.682G>C
|
ENSP00000510410.1:p.Asp228His
|
|
ENST00000691812.1:c.784G>C
|
ENSP00000510211.1:p.Asp262His
|
|
ENST00000693759.1:c.*396G>C
|
ENSP00000509518.1:n.*396G>C
|
|
ENST00000370803.8:c.784G>C
MANE Select
|
ENSP00000359839.4:p.Asp262His
|
|
ENST00000332070.7:c.784G>C
|
ENSP00000329097.3:p.Asp262His
|
|
ENST00000370799.5:c.787G>C
|
ENSP00000359835.1:p.Asp263His
|
|
ENST00000370800.4:c.787G>C
|
ENSP00000359836.4:p.Asp263His
|
|
ENST00000370803.7:c.784G>C
|
ENSP00000359839.3:p.Asp262His
|
|
ENST00000625464.2:c.787G>C
|
ENSP00000487420.1:p.Asp263His
|
|
NM_001015877.1:c.784G>C , LRG_629t1:c.784G>C
|
NP_001015877.1:p.Asp262His
|
|
NM_032335.3:c.787G>C , LRG_629t2:c.787G>C
|
NP_115711.2:p.Asp263His
|
|
NM_032458.2:c.784G>C
|
NP_115834.1:p.Asp262His
|
|
NM_001015877.2:c.784G>C
MANE Select
|
NP_001015877.1:p.Asp262His
|
|
NM_032458.3:c.784G>C
|
NP_115834.1:p.Asp262His
|
|