ENST00000436784.7:c.1556T>G
MANE Select
|
ENSP00000389175.2:p.Phe519Cys
|
|
ENST00000436784.6:c.1556T>G
|
ENSP00000389175.2:p.Phe519Cys
|
|
ENST00000461183.5:c.828T>G
|
ENSP00000417264.1:p.Val276=
|
|
ENST00000471180.5:c.699T>G
|
ENSP00000417526.1:p.Val233=
|
|
ENST00000473032.5:c.594T>G
|
ENSP00000418951.1:p.Val198=
|
|
ENST00000486393.5:c.*919T>G
|
ENSP00000419868.1:n.*919T>G
|
|
ENST00000489173.1:n.1850T>G
|
|
|
NM_145262.3:c.1556T>G
|
NP_660305.2:p.Phe519Cys
|
|
NR_026699.1:n.1654T>G
|
|
|
NR_026700.1:n.760T>G
|
|
|
NR_026701.1:n.1652T>G
|
|
|
NR_026702.1:n.690T>G
|
|
|
XM_005264878.2:c.*675T>G
|
XP_005264935.1:n.*675T>G
|
|
XR_245095.2:n.2807T>G
|
|
|
XM_017005730.1:c.1175T>G
|
XP_016861219.1:p.Phe392Cys
|
|
XM_024453351.1:c.1556T>G
|
XP_024309119.1:p.Phe519Cys
|
|
XM_024453352.1:c.*675T>G
|
XP_024309120.1:n.*675T>G
|
|
XR_001740022.2:n.3458T>G
|
|
|
XR_001740023.2:n.2982T>G
|
|
|
XR_245095.4:n.2808T>G
|
|
|
NM_145262.4:c.1556T>G
MANE Select
|
NP_660305.2:p.Phe519Cys
|
|
NR_026699.2:n.1646T>G
|
|
|
NR_026700.2:n.752T>G
|
|
|
NR_026701.2:n.1644T>G
|
|
|
NR_026702.2:n.682T>G
|
|
|
NM_001144951.2:c.*675T>G
|
NP_001138423.1:n.*675T>G
|
|