ENST00000291074.10:c.*126A>G
|
ENSP00000291074.5:n.*126A>G
|
|
ENST00000437048.7:c.2085+141A>G
MANE Select
|
ENSP00000401435.2:n.2085+141A>G
|
|
ENST00000571805.6:c.*126A>G
|
ENSP00000459312.1:n.*126A>G
|
|
ENST00000680128.1:c.*126A>G
|
ENSP00000506159.1:n.*126A>G
|
|
ENST00000680465.1:c.2085+141A>G
|
ENSP00000505997.1:n.2085+141A>G
|
|
ENST00000680641.1:c.*3334+141A>G
|
ENSP00000505237.1:n.*3334+141A>G
|
|
ENST00000680872.1:c.*1211+141A>G
|
ENSP00000506605.1:n.*1211+141A>G
|
|
ENST00000681050.1:c.298+141A>G
|
|
|
ENST00000681096.1:c.*126A>G
|
ENSP00000506052.1:n.*126A>G
|
|
ENST00000681103.1:c.315+141A>G
|
ENSP00000505892.1:n.315+141A>G
|
|
ENST00000681160.1:c.1716+141A>G
|
ENSP00000504905.1:n.1716+141A>G
|
|
ENST00000681317.1:c.2015+4327A>G
|
ENSP00000505190.1:n.2015+4327A>G
|
|
ENST00000681478.1:c.*2046A>G
|
ENSP00000505041.1:n.*2046A>G
|
|
ENST00000681510.1:c.1935+141A>G
|
ENSP00000505594.1:n.1935+141A>G
|
|
ENST00000681600.1:n.1180+141A>G
|
|
|
ENST00000681661.1:c.*1066+141A>G
|
ENSP00000506596.1:n.*1066+141A>G
|
|
ENST00000681858.1:c.315+141A>G
|
ENSP00000505044.1:n.315+141A>G
|
|
ENST00000681917.1:c.1554+141A>G
|
ENSP00000505944.1:n.1554+141A>G
|
|
ENST00000681943.1:c.1803+141A>G
|
ENSP00000504889.1:n.1803+141A>G
|
|
ENST00000681946.1:c.*1066+141A>G
|
ENSP00000505563.1:n.*1066+141A>G
|
|
ENST00000291074.9:c.*126A>G
|
ENSP00000291074.5:n.*126A>G
|
|
ENST00000437048.6:c.2085+141A>G
|
ENSP00000401435.2:n.2085+141A>G
|
|
ENST00000570771.1:n.152+141A>G
|
|
|
ENST00000573028.5:c.*1673A>G
|
ENSP00000458311.1:n.*1673A>G
|
|
ENST00000574029.5:c.207-15062A>G
|
ENSP00000459159.1:n.207-15062A>G
|
|
ENST00000576149.5:n.1855+141A>G
|
|
|
NM_001128159.2:c.2085+141A>G
|
NP_001121631.1:n.2085+141A>G
|
|
NM_018289.3:c.*126A>G
|
NP_060759.2:n.*126A>G
|
|
XR_934061.1:n.2382+141A>G
|
|
|
XR_934133.1:n.291-7688T>C
|
|
|
XM_017024817.2:c.1935+141A>G
|
XP_016880306.1:n.1935+141A>G
|
|
XM_017024818.1:c.1716+141A>G
|
XP_016880307.1:n.1716+141A>G
|
|
XR_001752553.2:n.2222+141A>G
|
|
|
XR_934061.3:n.2372+141A>G
|
|
|
NM_001128159.3:c.2085+141A>G
MANE Select
|
NP_001121631.1:n.2085+141A>G
|
|
NM_001366253.2:c.*126A>G
|
NP_001353182.1:n.*126A>G
|
|
NM_001366254.2:c.*126A>G
|
NP_001353183.1:n.*126A>G
|
|
NM_018289.4:c.*126A>G
|
NP_060759.2:n.*126A>G
|
|