ENST00000436784.7:c.1377G>T
MANE Select
|
ENSP00000389175.2:p.Glu459Asp
|
|
ENST00000305690.12:c.*496G>T
|
ENSP00000301965.9:n.*496G>T
|
|
ENST00000436784.6:c.1377G>T
|
ENSP00000389175.2:p.Glu459Asp
|
|
ENST00000461183.5:c.764-115G>T
|
ENSP00000417264.1:n.764-115G>T
|
|
ENST00000471180.5:c.635-115G>T
|
ENSP00000417526.1:n.635-115G>T
|
|
ENST00000473032.5:c.530-115G>T
|
ENSP00000418951.1:n.530-115G>T
|
|
ENST00000477382.1:c.*496G>T
|
ENSP00000419008.1:n.*496G>T
|
|
ENST00000486393.5:c.*740G>T
|
ENSP00000419868.1:n.*740G>T
|
|
ENST00000489173.1:n.1671G>T
|
|
|
NM_001144951.1:c.*496G>T
|
NP_001138423.1:n.*496G>T
|
|
NM_145262.3:c.1377G>T
|
NP_660305.2:p.Glu459Asp
|
|
NR_026699.1:n.1475G>T
|
|
|
NR_026700.1:n.696-115G>T
|
|
|
NR_026701.1:n.1473G>T
|
|
|
NR_026702.1:n.626-115G>T
|
|
|
XM_005264878.2:c.*496G>T
|
XP_005264935.1:n.*496G>T
|
|
XR_245095.2:n.2743-115G>T
|
|
|
XM_017005730.1:c.996G>T
|
XP_016861219.1:p.Glu332Asp
|
|
XM_024453351.1:c.1377G>T
|
XP_024309119.1:p.Glu459Asp
|
|
XM_024453352.1:c.*496G>T
|
XP_024309120.1:n.*496G>T
|
|
XR_001740022.2:n.3279G>T
|
|
|
XR_001740023.2:n.2918-115G>T
|
|
|
XR_245095.4:n.2744-115G>T
|
|
|
NM_145262.4:c.1377G>T
MANE Select
|
NP_660305.2:p.Glu459Asp
|
|
NR_026699.2:n.1467G>T
|
|
|
NR_026700.2:n.688-115G>T
|
|
|
NR_026701.2:n.1465G>T
|
|
|
NR_026702.2:n.618-115G>T
|
|
|
NM_001144951.2:c.*496G>T
|
NP_001138423.1:n.*496G>T
|
|