ENST00000436784.7:c.1553T>G
MANE Select
|
ENSP00000389175.2:p.Leu518Trp
|
|
ENST00000436784.6:c.1553T>G
|
ENSP00000389175.2:p.Leu518Trp
|
|
ENST00000461183.5:c.825T>G
|
ENSP00000417264.1:p.Leu275=
|
|
ENST00000471180.5:c.696T>G
|
ENSP00000417526.1:p.Leu232=
|
|
ENST00000473032.5:c.591T>G
|
ENSP00000418951.1:p.Leu197=
|
|
ENST00000486393.5:c.*916T>G
|
ENSP00000419868.1:n.*916T>G
|
|
ENST00000489173.1:n.1847T>G
|
|
|
NM_145262.3:c.1553T>G
|
NP_660305.2:p.Leu518Trp
|
|
NR_026699.1:n.1651T>G
|
|
|
NR_026700.1:n.757T>G
|
|
|
NR_026701.1:n.1649T>G
|
|
|
NR_026702.1:n.687T>G
|
|
|
XM_005264878.2:c.*672T>G
|
XP_005264935.1:n.*672T>G
|
|
XR_245095.2:n.2804T>G
|
|
|
XM_017005730.1:c.1172T>G
|
XP_016861219.1:p.Leu391Trp
|
|
XM_024453351.1:c.1553T>G
|
XP_024309119.1:p.Leu518Trp
|
|
XM_024453352.1:c.*672T>G
|
XP_024309120.1:n.*672T>G
|
|
XR_001740022.2:n.3455T>G
|
|
|
XR_001740023.2:n.2979T>G
|
|
|
XR_245095.4:n.2805T>G
|
|
|
NM_145262.4:c.1553T>G
MANE Select
|
NP_660305.2:p.Leu518Trp
|
|
NR_026699.2:n.1643T>G
|
|
|
NR_026700.2:n.749T>G
|
|
|
NR_026701.2:n.1641T>G
|
|
|
NR_026702.2:n.679T>G
|
|
|
NM_001144951.2:c.*672T>G
|
NP_001138423.1:n.*672T>G
|
|