ENST00000685553.1:c.*711T>C
|
ENSP00000510193.1:n.*711T>C
|
|
ENST00000687496.1:c.690T>C
|
ENSP00000509551.1:p.Asp230=
|
|
ENST00000688598.1:c.690T>C
|
ENSP00000510410.1:p.Asp230=
|
|
ENST00000691812.1:c.792T>C
|
ENSP00000510211.1:p.Asp264=
|
|
ENST00000693759.1:c.*404T>C
|
ENSP00000509518.1:n.*404T>C
|
|
ENST00000370803.8:c.792T>C
MANE Select
|
ENSP00000359839.4:p.Asp264=
|
|
ENST00000332070.7:c.792T>C
|
ENSP00000329097.3:p.Asp264=
|
|
ENST00000370799.5:c.795T>C
|
ENSP00000359835.1:p.Asp265=
|
|
ENST00000370800.4:c.795T>C
|
ENSP00000359836.4:p.Asp265=
|
|
ENST00000370803.7:c.792T>C
|
ENSP00000359839.3:p.Asp264=
|
|
ENST00000625464.2:c.795T>C
|
ENSP00000487420.1:p.Asp265=
|
|
NM_001015877.1:c.792T>C , LRG_629t1:c.792T>C
|
NP_001015877.1:p.Asp264=
|
|
NM_032335.3:c.795T>C , LRG_629t2:c.795T>C
|
NP_115711.2:p.Asp265=
|
|
NM_032458.2:c.792T>C
|
NP_115834.1:p.Asp264=
|
|
NM_001015877.2:c.792T>C
MANE Select
|
NP_001015877.1:p.Asp264=
|
|
NM_032458.3:c.792T>C
|
NP_115834.1:p.Asp264=
|
|