ENST00000436784.7:c.1171G>T
MANE Select
|
ENSP00000389175.2:p.Ala391Ser
|
|
ENST00000305690.12:c.*290G>T
|
ENSP00000301965.9:n.*290G>T
|
|
ENST00000436784.6:c.1171G>T
|
ENSP00000389175.2:p.Ala391Ser
|
|
ENST00000461183.5:c.763+156G>T
|
ENSP00000417264.1:n.763+156G>T
|
|
ENST00000471180.5:c.634+156G>T
|
ENSP00000417526.1:n.634+156G>T
|
|
ENST00000473032.5:c.530-321G>T
|
ENSP00000418951.1:n.530-321G>T
|
|
ENST00000477382.1:c.*290G>T
|
ENSP00000419008.1:n.*290G>T
|
|
ENST00000486393.5:c.*534G>T
|
ENSP00000419868.1:n.*534G>T
|
|
ENST00000489173.1:n.1465G>T
|
|
|
NM_001144951.1:c.*290G>T
|
NP_001138423.1:n.*290G>T
|
|
NM_145262.3:c.1171G>T
|
NP_660305.2:p.Ala391Ser
|
|
NR_026699.1:n.1269G>T
|
|
|
NR_026700.1:n.695+156G>T
|
|
|
NR_026701.1:n.1267G>T
|
|
|
NR_026702.1:n.626-321G>T
|
|
|
XM_005264878.2:c.*290G>T
|
XP_005264935.1:n.*290G>T
|
|
XR_245095.2:n.2742+156G>T
|
|
|
XM_017005730.1:c.790G>T
|
XP_016861219.1:p.Ala264Ser
|
|
XM_024453351.1:c.1171G>T
|
XP_024309119.1:p.Ala391Ser
|
|
XM_024453352.1:c.*290G>T
|
XP_024309120.1:n.*290G>T
|
|
XR_001740022.2:n.3073G>T
|
|
|
XR_001740023.2:n.2917+156G>T
|
|
|
XR_245095.4:n.2743+156G>T
|
|
|
NM_145262.4:c.1171G>T
MANE Select
|
NP_660305.2:p.Ala391Ser
|
|
NR_026699.2:n.1261G>T
|
|
|
NR_026700.2:n.687+156G>T
|
|
|
NR_026701.2:n.1259G>T
|
|
|
NR_026702.2:n.618-321G>T
|
|
|
NM_001144951.2:c.*290G>T
|
NP_001138423.1:n.*290G>T
|
|