ENST00000436784.7:c.1548C>T
MANE Select
|
ENSP00000389175.2:p.His516=
|
|
ENST00000436784.6:c.1548C>T
|
ENSP00000389175.2:p.His516=
|
|
ENST00000461183.5:c.820C>T
|
ENSP00000417264.1:p.Pro274Ser
|
|
ENST00000471180.5:c.691C>T
|
ENSP00000417526.1:p.Pro231Ser
|
|
ENST00000473032.5:c.586C>T
|
ENSP00000418951.1:p.Pro196Ser
|
|
ENST00000486393.5:c.*911C>T
|
ENSP00000419868.1:n.*911C>T
|
|
ENST00000489173.1:n.1842C>T
|
|
|
NM_145262.3:c.1548C>T
|
NP_660305.2:p.His516=
|
|
NR_026699.1:n.1646C>T
|
|
|
NR_026700.1:n.752C>T
|
|
|
NR_026701.1:n.1644C>T
|
|
|
NR_026702.1:n.682C>T
|
|
|
XM_005264878.2:c.*667C>T
|
XP_005264935.1:n.*667C>T
|
|
XR_245095.2:n.2799C>T
|
|
|
XM_017005730.1:c.1167C>T
|
XP_016861219.1:p.His389=
|
|
XM_024453351.1:c.1548C>T
|
XP_024309119.1:p.His516=
|
|
XM_024453352.1:c.*667C>T
|
XP_024309120.1:n.*667C>T
|
|
XR_001740022.2:n.3450C>T
|
|
|
XR_001740023.2:n.2974C>T
|
|
|
XR_245095.4:n.2800C>T
|
|
|
NM_145262.4:c.1548C>T
MANE Select
|
NP_660305.2:p.His516=
|
|
NR_026699.2:n.1638C>T
|
|
|
NR_026700.2:n.744C>T
|
|
|
NR_026701.2:n.1636C>T
|
|
|
NR_026702.2:n.674C>T
|
|
|
NM_001144951.2:c.*667C>T
|
NP_001138423.1:n.*667C>T
|
|