ENST00000436784.7:c.1565C>A
MANE Select
|
ENSP00000389175.2:p.Pro522His
|
|
ENST00000436784.6:c.1565C>A
|
ENSP00000389175.2:p.Pro522His
|
|
ENST00000461183.5:c.837C>A
|
ENSP00000417264.1:p.Ala279=
|
|
ENST00000471180.5:c.708C>A
|
ENSP00000417526.1:p.Ala236=
|
|
ENST00000473032.5:c.603C>A
|
ENSP00000418951.1:p.Ala201=
|
|
ENST00000486393.5:c.*928C>A
|
ENSP00000419868.1:n.*928C>A
|
|
ENST00000489173.1:n.1859C>A
|
|
|
NM_145262.3:c.1565C>A
|
NP_660305.2:p.Pro522His
|
|
NR_026699.1:n.1663C>A
|
|
|
NR_026700.1:n.769C>A
|
|
|
NR_026701.1:n.1661C>A
|
|
|
NR_026702.1:n.699C>A
|
|
|
XM_005264878.2:c.*684C>A
|
XP_005264935.1:n.*684C>A
|
|
XR_245095.2:n.2816C>A
|
|
|
XM_017005730.1:c.1184C>A
|
XP_016861219.1:p.Pro395His
|
|
XM_024453351.1:c.1565C>A
|
XP_024309119.1:p.Pro522His
|
|
XM_024453352.1:c.*684C>A
|
XP_024309120.1:n.*684C>A
|
|
XR_001740022.2:n.3467C>A
|
|
|
XR_001740023.2:n.2991C>A
|
|
|
XR_245095.4:n.2817C>A
|
|
|
NM_145262.4:c.1565C>A
MANE Select
|
NP_660305.2:p.Pro522His
|
|
NR_026699.2:n.1655C>A
|
|
|
NR_026700.2:n.761C>A
|
|
|
NR_026701.2:n.1653C>A
|
|
|
NR_026702.2:n.691C>A
|
|
|
NM_001144951.2:c.*684C>A
|
NP_001138423.1:n.*684C>A
|
|