ENST00000393078.5:c.909G>T
MANE Select
|
ENSP00000376793.3:p.Leu303=
|
|
ENST00000393078.4:c.909G>T
|
ENSP00000376793.3:p.Leu303=
|
|
ENST00000393080.8:c.909G>T
|
ENSP00000376795.4:p.Leu303=
|
|
ENST00000467132.5:c.909G>T
|
ENSP00000450540.1:p.Leu303=
|
|
ENST00000482740.2:c.255G>T
|
ENSP00000451119.1:p.Leu85=
|
|
ENST00000553947.1:c.1872G>T
|
|
|
ENST00000555820.1:c.909G>T
|
ENSP00000452246.3:p.Leu303=
|
|
ENST00000556388.1:n.58-2881G>T
|
|
|
ENST00000556968.2:c.644-2881G>T
|
ENSP00000452476.1:n.644-2881G>T
|
|
ENST00000621603.1:c.128G>T
|
|
|
NM_001085.4:c.909G>T
|
NP_001076.2:p.Leu303=
|
|
NM_001085.5:c.909G>T
MANE Select
|
NP_001076.2:p.Leu303=
|
|
NM_001384672.1:c.909G>T
|
NP_001371601.1:p.Leu303=
|
|
NM_001384673.1:c.909G>T
|
NP_001371602.1:p.Leu303=
|
|
NM_001384674.1:c.909G>T
|
NP_001371603.1:p.Leu303=
|
|