ENST00000436784.7:c.1125T>A
MANE Select
|
ENSP00000389175.2:p.His375Gln
|
|
ENST00000305690.12:c.*244T>A
|
ENSP00000301965.9:n.*244T>A
|
|
ENST00000436784.6:c.1125T>A
|
ENSP00000389175.2:p.His375Gln
|
|
ENST00000461183.5:c.763+110T>A
|
ENSP00000417264.1:n.763+110T>A
|
|
ENST00000471180.5:c.634+110T>A
|
ENSP00000417526.1:n.634+110T>A
|
|
ENST00000473032.5:c.530-367T>A
|
ENSP00000418951.1:n.530-367T>A
|
|
ENST00000477382.1:c.*244T>A
|
ENSP00000419008.1:n.*244T>A
|
|
ENST00000486393.5:c.*488T>A
|
ENSP00000419868.1:n.*488T>A
|
|
ENST00000489173.1:n.1419T>A
|
|
|
NM_001144951.1:c.*244T>A
|
NP_001138423.1:n.*244T>A
|
|
NM_145262.3:c.1125T>A
|
NP_660305.2:p.His375Gln
|
|
NR_026699.1:n.1223T>A
|
|
|
NR_026700.1:n.695+110T>A
|
|
|
NR_026701.1:n.1221T>A
|
|
|
NR_026702.1:n.626-367T>A
|
|
|
XM_005264878.2:c.*244T>A
|
XP_005264935.1:n.*244T>A
|
|
XR_245095.2:n.2742+110T>A
|
|
|
XM_017005730.1:c.744T>A
|
XP_016861219.1:p.His248Gln
|
|
XM_024453351.1:c.1125T>A
|
XP_024309119.1:p.His375Gln
|
|
XM_024453352.1:c.*244T>A
|
XP_024309120.1:n.*244T>A
|
|
XR_001740022.2:n.3027T>A
|
|
|
XR_001740023.2:n.2917+110T>A
|
|
|
XR_245095.4:n.2743+110T>A
|
|
|
NM_145262.4:c.1125T>A
MANE Select
|
NP_660305.2:p.His375Gln
|
|
NR_026699.2:n.1215T>A
|
|
|
NR_026700.2:n.687+110T>A
|
|
|
NR_026701.2:n.1213T>A
|
|
|
NR_026702.2:n.618-367T>A
|
|
|
NM_001144951.2:c.*244T>A
|
NP_001138423.1:n.*244T>A
|
|