ENST00000436784.7:c.1464C>A
MANE Select
|
ENSP00000389175.2:p.Asp488Glu
|
|
ENST00000436784.6:c.1464C>A
|
ENSP00000389175.2:p.Asp488Glu
|
|
ENST00000461183.5:c.764-28C>A
|
ENSP00000417264.1:n.764-28C>A
|
|
ENST00000471180.5:c.635-28C>A
|
ENSP00000417526.1:n.635-28C>A
|
|
ENST00000473032.5:c.530-28C>A
|
ENSP00000418951.1:n.530-28C>A
|
|
ENST00000486393.5:c.*827C>A
|
ENSP00000419868.1:n.*827C>A
|
|
ENST00000489173.1:n.1758C>A
|
|
|
NM_145262.3:c.1464C>A
|
NP_660305.2:p.Asp488Glu
|
|
NR_026699.1:n.1562C>A
|
|
|
NR_026700.1:n.696-28C>A
|
|
|
NR_026701.1:n.1560C>A
|
|
|
NR_026702.1:n.626-28C>A
|
|
|
XM_005264878.2:c.*583C>A
|
XP_005264935.1:n.*583C>A
|
|
XR_245095.2:n.2743-28C>A
|
|
|
XM_017005730.1:c.1083C>A
|
XP_016861219.1:p.Asp361Glu
|
|
XM_024453351.1:c.1464C>A
|
XP_024309119.1:p.Asp488Glu
|
|
XM_024453352.1:c.*583C>A
|
XP_024309120.1:n.*583C>A
|
|
XR_001740022.2:n.3366C>A
|
|
|
XR_001740023.2:n.2918-28C>A
|
|
|
XR_245095.4:n.2744-28C>A
|
|
|
NM_145262.4:c.1464C>A
MANE Select
|
NP_660305.2:p.Asp488Glu
|
|
NR_026699.2:n.1554C>A
|
|
|
NR_026700.2:n.688-28C>A
|
|
|
NR_026701.2:n.1552C>A
|
|
|
NR_026702.2:n.618-28C>A
|
|
|
NM_001144951.2:c.*583C>A
|
NP_001138423.1:n.*583C>A
|
|