ENST00000436784.7:c.*6T>G
MANE Select
|
ENSP00000389175.2:n.*6T>G
|
|
ENST00000436784.6:c.*6T>G
|
ENSP00000389175.2:n.*6T>G
|
|
ENST00000461183.5:c.850T>G
|
ENSP00000417264.1:p.Ter284Glu
|
|
ENST00000471180.5:c.721T>G
|
ENSP00000417526.1:p.Ter241Glu
|
|
ENST00000473032.5:c.616T>G
|
ENSP00000418951.1:p.Ter206Glu
|
|
ENST00000486393.5:c.*941T>G
|
ENSP00000419868.1:n.*941T>G
|
|
ENST00000489173.1:n.1872T>G
|
|
|
NM_145262.3:c.*6T>G
|
NP_660305.2:n.*6T>G
|
|
NR_026699.1:n.1676T>G
|
|
|
NR_026700.1:n.782T>G
|
|
|
NR_026701.1:n.1674T>G
|
|
|
NR_026702.1:n.712T>G
|
|
|
XM_005264878.2:c.*697T>G
|
XP_005264935.1:n.*697T>G
|
|
XR_245095.2:n.2829T>G
|
|
|
XM_017005730.1:c.*6T>G
|
XP_016861219.1:n.*6T>G
|
|
XM_024453351.1:c.*6T>G
|
XP_024309119.1:n.*6T>G
|
|
XM_024453352.1:c.*697T>G
|
XP_024309120.1:n.*697T>G
|
|
XR_001740022.2:n.3480T>G
|
|
|
XR_001740023.2:n.3004T>G
|
|
|
XR_245095.4:n.2830T>G
|
|
|
NM_145262.4:c.*6T>G
MANE Select
|
NP_660305.2:n.*6T>G
|
|
NR_026699.2:n.1668T>G
|
|
|
NR_026700.2:n.774T>G
|
|
|
NR_026701.2:n.1666T>G
|
|
|
NR_026702.2:n.704T>G
|
|
|
NM_001144951.2:c.*697T>G
|
NP_001138423.1:n.*697T>G
|
|