ENST00000436784.7:c.1546del
MANE Select
|
ENSP00000389175.2:p.His516ThrfsTer?
|
|
ENST00000436784.6:c.1546del
|
ENSP00000389175.2:p.His516ThrfsTer?
|
|
ENST00000461183.5:c.818del
|
ENSP00000417264.1:p.Pro273HisfsTer9
|
|
ENST00000471180.5:c.689del
|
ENSP00000417526.1:p.Pro230HisfsTer9
|
|
ENST00000473032.5:c.584del
|
ENSP00000418951.1:p.Pro195HisfsTer9
|
|
ENST00000486393.5:c.*909del
|
ENSP00000419868.1:n.*909del
|
|
ENST00000489173.1:n.1840del
|
|
|
NM_145262.3:c.1546del
|
NP_660305.2:p.His516ThrfsTer?
|
|
NR_026699.1:n.1644del
|
|
|
NR_026700.1:n.750del
|
|
|
NR_026701.1:n.1642del
|
|
|
NR_026702.1:n.680del
|
|
|
XM_005264878.2:c.*665del
|
XP_005264935.1:n.*665del
|
|
XR_245095.2:n.2797del
|
|
|
XM_017005730.1:c.1165del
|
XP_016861219.1:p.His389ThrfsTer?
|
|
XM_024453351.1:c.1546del
|
XP_024309119.1:p.His516ThrfsTer?
|
|
XM_024453352.1:c.*665del
|
XP_024309120.1:n.*665del
|
|
XR_001740022.2:n.3448del
|
|
|
XR_001740023.2:n.2972del
|
|
|
XR_245095.4:n.2798del
|
|
|
NM_145262.4:c.1546del
MANE Select
|
NP_660305.2:p.His516ThrfsTer?
|
|
NR_026699.2:n.1636del
|
|
|
NR_026700.2:n.742del
|
|
|
NR_026701.2:n.1634del
|
|
|
NR_026702.2:n.672del
|
|
|
NM_001144951.2:c.*665del
|
NP_001138423.1:n.*665del
|
|