ENST00000436784.7:c.1545C>T
MANE Select
|
ENSP00000389175.2:p.Thr515=
|
|
ENST00000436784.6:c.1545C>T
|
ENSP00000389175.2:p.Thr515=
|
|
ENST00000461183.5:c.817C>T
|
ENSP00000417264.1:p.Pro273Ser
|
|
ENST00000471180.5:c.688C>T
|
ENSP00000417526.1:p.Pro230Ser
|
|
ENST00000473032.5:c.583C>T
|
ENSP00000418951.1:p.Pro195Ser
|
|
ENST00000486393.5:c.*908C>T
|
ENSP00000419868.1:n.*908C>T
|
|
ENST00000489173.1:n.1839C>T
|
|
|
NM_145262.3:c.1545C>T
|
NP_660305.2:p.Thr515=
|
|
NR_026699.1:n.1643C>T
|
|
|
NR_026700.1:n.749C>T
|
|
|
NR_026701.1:n.1641C>T
|
|
|
NR_026702.1:n.679C>T
|
|
|
XM_005264878.2:c.*664C>T
|
XP_005264935.1:n.*664C>T
|
|
XR_245095.2:n.2796C>T
|
|
|
XM_017005730.1:c.1164C>T
|
XP_016861219.1:p.Thr388=
|
|
XM_024453351.1:c.1545C>T
|
XP_024309119.1:p.Thr515=
|
|
XM_024453352.1:c.*664C>T
|
XP_024309120.1:n.*664C>T
|
|
XR_001740022.2:n.3447C>T
|
|
|
XR_001740023.2:n.2971C>T
|
|
|
XR_245095.4:n.2797C>T
|
|
|
NM_145262.4:c.1545C>T
MANE Select
|
NP_660305.2:p.Thr515=
|
|
NR_026699.2:n.1635C>T
|
|
|
NR_026700.2:n.741C>T
|
|
|
NR_026701.2:n.1633C>T
|
|
|
NR_026702.2:n.671C>T
|
|
|
NM_001144951.2:c.*664C>T
|
NP_001138423.1:n.*664C>T
|
|