ENST00000685553.1:c.*510T=
|
ENSP00000510193.1:n.*510T=
|
|
ENST00000687496.1:c.489T=
|
ENSP00000509551.1:p.Asp163=
|
|
ENST00000688598.1:c.489T=
|
ENSP00000510410.1:p.Asp163=
|
|
ENST00000691812.1:c.591T=
|
ENSP00000510211.1:p.Asp197=
|
|
ENST00000693759.1:c.*203T=
|
ENSP00000509518.1:n.*203T=
|
|
ENST00000370803.8:c.591T=
MANE Select
|
ENSP00000359839.4:p.Asp197=
|
|
ENST00000332070.7:c.591T=
|
ENSP00000329097.3:p.Asp197=
|
|
ENST00000370799.5:c.594T=
|
ENSP00000359835.1:p.Asp198=
|
|
ENST00000370800.4:c.594T=
|
ENSP00000359836.4:p.Asp198=
|
|
ENST00000370803.7:c.591T=
|
ENSP00000359839.3:p.Asp197=
|
|
ENST00000625464.2:c.594T=
|
ENSP00000487420.1:p.Asp198=
|
|
NM_001015877.1:c.591T= , LRG_629t1:c.591T=
|
NP_001015877.1:p.Asp197=
|
|
NM_032335.3:c.594T= , LRG_629t2:c.594T=
|
NP_115711.2:p.Asp198=
|
|
NM_032458.2:c.591T=
|
NP_115834.1:p.Asp197=
|
|
NM_001015877.2:c.591T=
MANE Select
|
NP_001015877.1:p.Asp197=
|
|
NM_032458.3:c.591T=
|
NP_115834.1:p.Asp197=
|
|