ENST00000436784.7:c.*8G>T
MANE Select
|
ENSP00000389175.2:n.*8G>T
|
|
ENST00000436784.6:c.*8G>T
|
ENSP00000389175.2:n.*8G>T
|
|
ENST00000461183.5:c.852G>T
|
ENSP00000417264.1:p.Ter284Tyr
|
|
ENST00000471180.5:c.723G>T
|
ENSP00000417526.1:p.Ter241Tyr
|
|
ENST00000473032.5:c.618G>T
|
ENSP00000418951.1:p.Ter206Tyr
|
|
ENST00000486393.5:c.*943G>T
|
ENSP00000419868.1:n.*943G>T
|
|
ENST00000489173.1:n.1874G>T
|
|
|
NM_145262.3:c.*8G>T
|
NP_660305.2:n.*8G>T
|
|
NR_026699.1:n.1678G>T
|
|
|
NR_026700.1:n.784G>T
|
|
|
NR_026701.1:n.1676G>T
|
|
|
NR_026702.1:n.714G>T
|
|
|
XM_005264878.2:c.*699G>T
|
XP_005264935.1:n.*699G>T
|
|
XR_245095.2:n.2831G>T
|
|
|
XM_017005730.1:c.*8G>T
|
XP_016861219.1:n.*8G>T
|
|
XM_024453351.1:c.*8G>T
|
XP_024309119.1:n.*8G>T
|
|
XM_024453352.1:c.*699G>T
|
XP_024309120.1:n.*699G>T
|
|
XR_001740022.2:n.3482G>T
|
|
|
XR_001740023.2:n.3006G>T
|
|
|
XR_245095.4:n.2832G>T
|
|
|
NM_145262.4:c.*8G>T
MANE Select
|
NP_660305.2:n.*8G>T
|
|
NR_026699.2:n.1670G>T
|
|
|
NR_026700.2:n.776G>T
|
|
|
NR_026701.2:n.1668G>T
|
|
|
NR_026702.2:n.706G>T
|
|
|
NM_001144951.2:c.*699G>T
|
NP_001138423.1:n.*699G>T
|
|