ENST00000436784.7:c.1555T>G
MANE Select
|
ENSP00000389175.2:p.Phe519Val
|
|
ENST00000436784.6:c.1555T>G
|
ENSP00000389175.2:p.Phe519Val
|
|
ENST00000461183.5:c.827T>G
|
ENSP00000417264.1:p.Val276Gly
|
|
ENST00000471180.5:c.698T>G
|
ENSP00000417526.1:p.Val233Gly
|
|
ENST00000473032.5:c.593T>G
|
ENSP00000418951.1:p.Val198Gly
|
|
ENST00000486393.5:c.*918T>G
|
ENSP00000419868.1:n.*918T>G
|
|
ENST00000489173.1:n.1849T>G
|
|
|
NM_145262.3:c.1555T>G
|
NP_660305.2:p.Phe519Val
|
|
NR_026699.1:n.1653T>G
|
|
|
NR_026700.1:n.759T>G
|
|
|
NR_026701.1:n.1651T>G
|
|
|
NR_026702.1:n.689T>G
|
|
|
XM_005264878.2:c.*674T>G
|
XP_005264935.1:n.*674T>G
|
|
XR_245095.2:n.2806T>G
|
|
|
XM_017005730.1:c.1174T>G
|
XP_016861219.1:p.Phe392Val
|
|
XM_024453351.1:c.1555T>G
|
XP_024309119.1:p.Phe519Val
|
|
XM_024453352.1:c.*674T>G
|
XP_024309120.1:n.*674T>G
|
|
XR_001740022.2:n.3457T>G
|
|
|
XR_001740023.2:n.2981T>G
|
|
|
XR_245095.4:n.2807T>G
|
|
|
NM_145262.4:c.1555T>G
MANE Select
|
NP_660305.2:p.Phe519Val
|
|
NR_026699.2:n.1645T>G
|
|
|
NR_026700.2:n.751T>G
|
|
|
NR_026701.2:n.1643T>G
|
|
|
NR_026702.2:n.681T>G
|
|
|
NM_001144951.2:c.*674T>G
|
NP_001138423.1:n.*674T>G
|
|