ENST00000340855.11:c.567G>A
MANE Select
|
ENSP00000339801.6:p.Leu189=
|
|
ENST00000651111.1:c.-67G>A
|
ENSP00000498395.1:n.-67G>A
|
|
ENST00000340855.10:c.567G>A
|
ENSP00000339801.6:p.Leu189=
|
|
ENST00000370441.8:c.567G>A
|
ENSP00000359470.4:p.Leu189=
|
|
ENST00000422081.6:c.-67G>A
|
ENSP00000477056.1:n.-67G>A
|
|
ENST00000441880.1:n.114-11150G>A
|
|
|
ENST00000464251.5:c.493G>A
|
ENSP00000428980.1:n.493G>A
|
|
ENST00000466019.1:n.19G>A
|
|
|
ENST00000466323.5:c.567G>A
|
ENSP00000418264.1:p.Leu189=
|
|
ENST00000490775.5:n.352G>A
|
|
|
ENST00000523759.5:n.681G>A
|
|
|
NM_000202.6:c.567G>A
|
NP_000193.1:p.Leu189=
|
|
NM_001166550.2:c.297G>A
|
NP_001160022.1:p.Leu99=
|
|
NM_006123.4:c.567G>A
|
NP_006114.1:p.Leu189=
|
|
NR_104128.1:n.784G>A
|
|
|
NM_000202.7:c.567G>A
|
NP_000193.1:p.Leu189=
|
|
NM_001166550.3:c.297G>A
|
NP_001160022.1:p.Leu99=
|
|
NM_000202.8:c.567G>A
MANE Select
|
NP_000193.1:p.Leu189=
|
|
NM_001166550.4:c.297G>A
|
NP_001160022.1:p.Leu99=
|
|
NM_006123.5:c.567G>A
|
NP_006114.1:p.Leu189=
|
|
NR_104128.2:n.736G>A
|
|
|