ENST00000257904.11:c.618G>A
MANE Select
|
ENSP00000257904.5:p.Glu206=
|
|
ENST00000257904.10:c.618G>A
|
ENSP00000257904.5:p.Glu206=
|
|
ENST00000312990.10:c.266G>A
|
ENSP00000316889.6:p.Arg89Lys
|
|
ENST00000546489.5:c.396G>A
|
ENSP00000447779.1:p.Glu132=
|
|
ENST00000547281.5:c.396G>A
|
ENSP00000447274.1:p.Glu132=
|
|
ENST00000549606.5:c.-157-1166G>A
|
ENSP00000447005.1:n.-157-1166G>A
|
|
ENST00000550419.5:c.523-107G>A
|
ENSP00000448098.1:n.523-107G>A
|
|
ENST00000551800.5:c.396G>A
|
ENSP00000449391.1:p.Glu132=
|
|
ENST00000551888.5:n.444G>A
|
|
|
ENST00000553237.5:c.*257G>A
|
ENSP00000448885.1:n.*257G>A
|
|
NM_000075.3:c.618G>A
|
NP_000066.1:p.Glu206=
|
|
NM_000075.4:c.618G>A
MANE Select
|
NP_000066.1:p.Glu206=
|
|