ENST00000436784.7:c.*6T>A
MANE Select
|
ENSP00000389175.2:n.*6T>A
|
|
ENST00000436784.6:c.*6T>A
|
ENSP00000389175.2:n.*6T>A
|
|
ENST00000461183.5:c.850T>A
|
ENSP00000417264.1:p.Ter284Lys
|
|
ENST00000471180.5:c.721T>A
|
ENSP00000417526.1:p.Ter241Lys
|
|
ENST00000473032.5:c.616T>A
|
ENSP00000418951.1:p.Ter206Lys
|
|
ENST00000486393.5:c.*941T>A
|
ENSP00000419868.1:n.*941T>A
|
|
ENST00000489173.1:n.1872T>A
|
|
|
NM_145262.3:c.*6T>A
|
NP_660305.2:n.*6T>A
|
|
NR_026699.1:n.1676T>A
|
|
|
NR_026700.1:n.782T>A
|
|
|
NR_026701.1:n.1674T>A
|
|
|
NR_026702.1:n.712T>A
|
|
|
XM_005264878.2:c.*697T>A
|
XP_005264935.1:n.*697T>A
|
|
XR_245095.2:n.2829T>A
|
|
|
XM_017005730.1:c.*6T>A
|
XP_016861219.1:n.*6T>A
|
|
XM_024453351.1:c.*6T>A
|
XP_024309119.1:n.*6T>A
|
|
XM_024453352.1:c.*697T>A
|
XP_024309120.1:n.*697T>A
|
|
XR_001740022.2:n.3480T>A
|
|
|
XR_001740023.2:n.3004T>A
|
|
|
XR_245095.4:n.2830T>A
|
|
|
NM_145262.4:c.*6T>A
MANE Select
|
NP_660305.2:n.*6T>A
|
|
NR_026699.2:n.1668T>A
|
|
|
NR_026700.2:n.774T>A
|
|
|
NR_026701.2:n.1666T>A
|
|
|
NR_026702.2:n.704T>A
|
|
|
NM_001144951.2:c.*697T>A
|
NP_001138423.1:n.*697T>A
|
|