ENST00000436784.7:c.1509G>T
MANE Select
|
ENSP00000389175.2:p.Leu503=
|
|
ENST00000436784.6:c.1509G>T
|
ENSP00000389175.2:p.Leu503=
|
|
ENST00000461183.5:c.781G>T
|
ENSP00000417264.1:p.Ala261Ser
|
|
ENST00000471180.5:c.652G>T
|
ENSP00000417526.1:p.Ala218Ser
|
|
ENST00000473032.5:c.547G>T
|
ENSP00000418951.1:p.Ala183Ser
|
|
ENST00000486393.5:c.*872G>T
|
ENSP00000419868.1:n.*872G>T
|
|
ENST00000489173.1:n.1803G>T
|
|
|
NM_145262.3:c.1509G>T
|
NP_660305.2:p.Leu503=
|
|
NR_026699.1:n.1607G>T
|
|
|
NR_026700.1:n.713G>T
|
|
|
NR_026701.1:n.1605G>T
|
|
|
NR_026702.1:n.643G>T
|
|
|
XM_005264878.2:c.*628G>T
|
XP_005264935.1:n.*628G>T
|
|
XR_245095.2:n.2760G>T
|
|
|
XM_017005730.1:c.1128G>T
|
XP_016861219.1:p.Leu376=
|
|
XM_024453351.1:c.1509G>T
|
XP_024309119.1:p.Leu503=
|
|
XM_024453352.1:c.*628G>T
|
XP_024309120.1:n.*628G>T
|
|
XR_001740022.2:n.3411G>T
|
|
|
XR_001740023.2:n.2935G>T
|
|
|
XR_245095.4:n.2761G>T
|
|
|
NM_145262.4:c.1509G>T
MANE Select
|
NP_660305.2:p.Leu503=
|
|
NR_026699.2:n.1599G>T
|
|
|
NR_026700.2:n.705G>T
|
|
|
NR_026701.2:n.1597G>T
|
|
|
NR_026702.2:n.635G>T
|
|
|
NM_001144951.2:c.*628G>T
|
NP_001138423.1:n.*628G>T
|
|