ENST00000232607.7:c.548T>A
MANE Select
|
ENSP00000232607.2:p.Leu183His
|
|
ENST00000232607.6:c.548T>A
|
ENSP00000232607.2:p.Leu183His
|
|
ENST00000460034.5:c.*292T>A
|
ENSP00000420409.1:n.*292T>A
|
|
ENST00000462091.5:c.*220T>A
|
ENSP00000417893.1:n.*220T>A
|
|
ENST00000467167.5:c.*446T>A
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ENSP00000419618.1:n.*446T>A
|
|
ENST00000474588.5:c.311-110T>A
|
ENSP00000420348.1:n.311-110T>A
|
|
ENST00000479719.5:c.548T>A
|
ENSP00000420754.1:p.Leu183His
|
|
ENST00000497791.5:c.*220T>A
|
ENSP00000419121.1:n.*220T>A
|
|
ENST00000498715.1:n.266T>A
|
|
|
NM_000373.3:c.548T>A
|
NP_000364.1:p.Leu183His
|
|
NR_033434.1:n.500T>A
|
|
|
NR_033437.1:n.753T>A
|
|
|
XR_001740253.2:n.578T>A
|
|
|
NM_000373.4:c.548T>A
MANE Select
|
NP_000364.1:p.Leu183His
|
|
NR_033434.2:n.414T>A
|
|
|
NR_033437.2:n.667T>A
|
|
|