ENST00000232607.7:c.545T>A
MANE Select
|
ENSP00000232607.2:p.Ile182Asn
|
|
ENST00000232607.6:c.545T>A
|
ENSP00000232607.2:p.Ile182Asn
|
|
ENST00000460034.5:c.*289T>A
|
ENSP00000420409.1:n.*289T>A
|
|
ENST00000462091.5:c.*217T>A
|
ENSP00000417893.1:n.*217T>A
|
|
ENST00000467167.5:c.*443T>A
|
ENSP00000419618.1:n.*443T>A
|
|
ENST00000474588.5:c.311-113T>A
|
ENSP00000420348.1:n.311-113T>A
|
|
ENST00000479719.5:c.545T>A
|
ENSP00000420754.1:p.Ile182Asn
|
|
ENST00000497791.5:c.*217T>A
|
ENSP00000419121.1:n.*217T>A
|
|
ENST00000498715.1:n.263T>A
|
|
|
NM_000373.3:c.545T>A
|
NP_000364.1:p.Ile182Asn
|
|
NR_033434.1:n.497T>A
|
|
|
NR_033437.1:n.750T>A
|
|
|
XR_001740253.2:n.575T>A
|
|
|
NM_000373.4:c.545T>A
MANE Select
|
NP_000364.1:p.Ile182Asn
|
|
NR_033434.2:n.411T>A
|
|
|
NR_033437.2:n.664T>A
|
|
|