ENST00000249806.11:c.881T>A
MANE Select
|
ENSP00000249806.5:p.Ile294Asn
|
|
ENST00000562767.2:c.84-10567T>A
|
ENSP00000456336.1:n.84-10567T>A
|
|
ENST00000565471.6:c.422T>A
|
ENSP00000457384.1:p.Ile141Asn
|
|
ENST00000635747.1:c.*784T>A
|
ENSP00000490627.1:n.*784T>A
|
|
ENST00000636212.1:c.*551T>A
|
ENSP00000489851.1:n.*551T>A
|
|
ENST00000636674.1:n.1983T>A
|
|
|
ENST00000636964.1:n.2409T>A
|
|
|
ENST00000637054.1:c.198+10341T>A
|
ENSP00000490807.1:n.198+10341T>A
|
|
ENST00000637329.1:c.850T>A
|
|
|
ENST00000637450.1:c.*535T>A
|
ENSP00000490204.1:n.*535T>A
|
|
ENST00000637494.1:c.593T>A
|
ENSP00000490057.1:p.Ile198Asn
|
|
ENST00000637823.1:c.706T>A
|
|
|
ENST00000637888.1:c.198+10341T>A
|
ENSP00000490546.1:n.198+10341T>A
|
|
ENST00000638076.1:c.*484T>A
|
ENSP00000490373.1:n.*484T>A
|
|
ENST00000638144.1:n.524T>A
|
|
|
ENST00000646164.1:c.39-8514T>A
|
|
|
ENST00000249806.9:c.881T>A
|
ENSP00000249806.5:p.Ile294Asn
|
|
ENST00000538696.5:c.977T>A
|
ENSP00000445770.1:p.Ile326Asn
|
|
ENST00000562767.1:c.84-10567T>A
|
ENSP00000456336.1:n.84-10567T>A
|
|
ENST00000565471.5:c.422T>A
|
ENSP00000457384.1:p.Ile141Asn
|
|
ENST00000566347.5:c.692T>A
|
ENSP00000457783.1:p.Ile231Asn
|
|
ENST00000567060.5:c.*279T>A
|
ENSP00000454818.1:n.*279T>A
|
|
NM_017882.2:c.881T>A
|
NP_060352.1:p.Ile294Asn
|
|
NM_017882.3:c.881T>A
MANE Select
|
NP_060352.1:p.Ile294Asn
|
|