|
ENST00000700029.2:c.934C>A
|
ENSP00000514759.2:p.Pro312Thr
|
|
|
ENST00000710265.1:c.841C>A
|
ENSP00000518161.1:p.Pro281Thr
|
|
|
ENST00000472832.3:c.841C>A
|
ENSP00000483066.2:p.Pro281Thr
|
|
|
ENST00000688158.2:n.1576C>A
|
|
|
|
ENST00000688922.2:c.*671C>A
|
ENSP00000508742.2:n.*671C>A
|
|
|
ENST00000700021.1:c.796C>A
|
ENSP00000514757.1:p.Pro266Thr
|
|
|
ENST00000700022.1:c.*180C>A
|
ENSP00000514758.1:n.*180C>A
|
|
|
ENST00000700023.1:n.1999C>A
|
|
|
|
ENST00000700024.1:n.2233C>A
|
|
|
|
ENST00000700025.1:n.1610C>A
|
|
|
|
ENST00000700026.1:n.478C>A
|
|
|
|
ENST00000700029.1:c.768C>A
|
|
|
|
ENST00000706954.1:c.841C>A
|
ENSP00000516674.1:p.Pro281Thr
|
|
|
ENST00000706955.1:c.*876C>A
|
ENSP00000516675.1:n.*876C>A
|
|
|
ENST00000686459.1:c.*427C>A
|
ENSP00000508909.1:n.*427C>A
|
|
|
ENST00000688158.1:c.*952C>A
|
ENSP00000509254.1:n.*952C>A
|
|
|
ENST00000688308.1:c.841C>A
|
ENSP00000508752.1:p.Pro281Thr
|
|
|
ENST00000688922.1:c.762C>A
|
|
|
|
ENST00000693560.1:c.1360C>A
|
ENSP00000509861.1:p.Pro454Thr
|
|
|
ENST00000371953.8:c.841C>A
MANE Select
|
ENSP00000361021.3:p.Pro281Thr
|
|
|
ENST00000371953.7:c.841C>A
|
ENSP00000361021.3:p.Pro281Thr
|
|
|
ENST00000472832.2:c.268C>A
|
ENSP00000483066.1:p.Pro90Thr
|
|
|
NM_000314.5:c.841C>A
|
NP_000305.3:p.Pro281Thr
|
|
|
NM_000314.6:c.841C>A
|
NP_000305.3:p.Pro281Thr
|
|
|
NM_001304717.2:c.1360C>A
|
NP_001291646.2:p.Pro454Thr
|
|
|
NM_001304718.1:c.250C>A
|
NP_001291647.1:p.Pro84Thr
|
|
|
XM_006717926.2:c.796C>A
|
XP_006717989.1:p.Pro266Thr
|
|
|
XM_011539981.1:c.841C>A
|
XP_011538283.1:p.Pro281Thr
|
|
|
XM_011539982.1:c.745C>A
|
XP_011538284.1:p.Pro249Thr
|
|
|
XR_945791.1:n.1411C>A
|
|
|
|
NM_000314.7:c.841C>A
|
NP_000305.3:p.Pro281Thr
|
|
|
NM_001304717.5:c.1360C>A
|
NP_001291646.4:p.Pro454Thr
|
|
|
NM_001304718.2:c.250C>A
|
NP_001291647.1:p.Pro84Thr
|
|
|
NM_000314.8:c.841C>A
MANE Select
|
NP_000305.3:p.Pro281Thr
|
|
