ENST00000636937.2:c.2766G>A
|
ENSP00000516154.1:p.Gln922=
|
|
ENST00000268124.11:c.2766G>A
MANE Select
|
ENSP00000268124.5:p.Gln922=
|
|
ENST00000530292.3:c.2367G>A
|
ENSP00000432885.2:p.Gln789=
|
|
ENST00000635986.2:c.2766G>A
|
ENSP00000490653.2:p.Gln922=
|
|
ENST00000636774.1:c.*1333G>A
|
ENSP00000489799.1:n.*1333G>A
|
|
ENST00000637238.1:c.1575G>A
|
ENSP00000490756.1:n.1575G>A
|
|
ENST00000637264.1:c.1838G>A
|
|
|
ENST00000666746.1:c.2343G>A
|
|
|
ENST00000670281.1:c.800+981G>A
|
ENSP00000499709.1:n.800+981G>A
|
|
ENST00000672071.1:n.2964G>A
|
|
|
ENST00000672923.2:n.2708G>A
|
|
|
ENST00000268124.9:c.2766G>A
|
ENSP00000268124.5:p.Gln922=
|
|
ENST00000442287.6:c.2766G>A
|
ENSP00000399851.2:p.Gln922=
|
|
ENST00000528881.2:c.363G>A
|
|
|
ENST00000530715.5:c.186-112G>A
|
ENSP00000431395.1:n.186-112G>A
|
|
ENST00000631044.2:c.*2190G>A
|
ENSP00000486730.1:n.*2190G>A
|
|
NM_001126131.1:c.2766G>A
|
NP_001119603.1:p.Gln922=
|
|
NM_002693.2:c.2766G>A
|
NP_002684.1:p.Gln922=
|
|
NM_001126131.2:c.2766G>A
|
NP_001119603.1:p.Gln922=
|
|
NM_002693.3:c.2766G>A
MANE Select
|
NP_002684.1:p.Gln922=
|
|