ENST00000393078.5:c.896_898delinsGGA
MANE Select
|
ENSP00000376793.3:p.Trp299=
|
|
ENST00000393078.4:c.896_898delinsGGA
|
ENSP00000376793.3:p.Trp299=
|
|
ENST00000393080.8:c.896_898delinsGGA
|
ENSP00000376795.4:p.Trp299=
|
|
ENST00000467132.5:c.896_898delinsGGA
|
ENSP00000450540.1:p.Trp299=
|
|
ENST00000482740.2:c.242_244delinsGGA
|
ENSP00000451119.1:p.Trp81=
|
|
ENST00000553947.1:c.1859_1861delinsGGA
|
|
|
ENST00000555820.1:c.896_898delinsGGA
|
ENSP00000452246.3:p.Trp299=
|
|
ENST00000556388.1:n.58-2894_58-2892delinsGGA
|
|
|
ENST00000556968.2:c.644-2894_644-2892delinsGGA
|
ENSP00000452476.1:n.644-2894_644-2892delinsGGA
|
|
ENST00000621603.1:c.115_117delinsGGA
|
|
|
NM_001085.4:c.896_898delinsGGA
|
NP_001076.2:p.Trp299=
|
|
NM_001085.5:c.896_898delinsGGA
MANE Select
|
NP_001076.2:p.Trp299=
|
|
NM_001384672.1:c.896_898delinsGGA
|
NP_001371601.1:p.Trp299=
|
|
NM_001384673.1:c.896_898delinsGGA
|
NP_001371602.1:p.Trp299=
|
|
NM_001384674.1:c.896_898delinsGGA
|
NP_001371603.1:p.Trp299=
|
|