ENST00000436784.7:c.1374A>T
MANE Select
|
ENSP00000389175.2:p.Thr458=
|
|
ENST00000305690.12:c.*493A>T
|
ENSP00000301965.9:n.*493A>T
|
|
ENST00000436784.6:c.1374A>T
|
ENSP00000389175.2:p.Thr458=
|
|
ENST00000461183.5:c.764-118A>T
|
ENSP00000417264.1:n.764-118A>T
|
|
ENST00000471180.5:c.635-118A>T
|
ENSP00000417526.1:n.635-118A>T
|
|
ENST00000473032.5:c.530-118A>T
|
ENSP00000418951.1:n.530-118A>T
|
|
ENST00000477382.1:c.*493A>T
|
ENSP00000419008.1:n.*493A>T
|
|
ENST00000486393.5:c.*737A>T
|
ENSP00000419868.1:n.*737A>T
|
|
ENST00000489173.1:n.1668A>T
|
|
|
NM_001144951.1:c.*493A>T
|
NP_001138423.1:n.*493A>T
|
|
NM_145262.3:c.1374A>T
|
NP_660305.2:p.Thr458=
|
|
NR_026699.1:n.1472A>T
|
|
|
NR_026700.1:n.696-118A>T
|
|
|
NR_026701.1:n.1470A>T
|
|
|
NR_026702.1:n.626-118A>T
|
|
|
XM_005264878.2:c.*493A>T
|
XP_005264935.1:n.*493A>T
|
|
XR_245095.2:n.2743-118A>T
|
|
|
XM_017005730.1:c.993A>T
|
XP_016861219.1:p.Thr331=
|
|
XM_024453351.1:c.1374A>T
|
XP_024309119.1:p.Thr458=
|
|
XM_024453352.1:c.*493A>T
|
XP_024309120.1:n.*493A>T
|
|
XR_001740022.2:n.3276A>T
|
|
|
XR_001740023.2:n.2918-118A>T
|
|
|
XR_245095.4:n.2744-118A>T
|
|
|
NM_145262.4:c.1374A>T
MANE Select
|
NP_660305.2:p.Thr458=
|
|
NR_026699.2:n.1464A>T
|
|
|
NR_026700.2:n.688-118A>T
|
|
|
NR_026701.2:n.1462A>T
|
|
|
NR_026702.2:n.618-118A>T
|
|
|
NM_001144951.2:c.*493A>T
|
NP_001138423.1:n.*493A>T
|
|