ENST00000436784.7:c.1560G>A
MANE Select
|
ENSP00000389175.2:p.Leu520=
|
|
ENST00000436784.6:c.1560G>A
|
ENSP00000389175.2:p.Leu520=
|
|
ENST00000461183.5:c.832G>A
|
ENSP00000417264.1:p.Ala278Thr
|
|
ENST00000471180.5:c.703G>A
|
ENSP00000417526.1:p.Ala235Thr
|
|
ENST00000473032.5:c.598G>A
|
ENSP00000418951.1:p.Ala200Thr
|
|
ENST00000486393.5:c.*923G>A
|
ENSP00000419868.1:n.*923G>A
|
|
ENST00000489173.1:n.1854G>A
|
|
|
NM_145262.3:c.1560G>A
|
NP_660305.2:p.Leu520=
|
|
NR_026699.1:n.1658G>A
|
|
|
NR_026700.1:n.764G>A
|
|
|
NR_026701.1:n.1656G>A
|
|
|
NR_026702.1:n.694G>A
|
|
|
XM_005264878.2:c.*679G>A
|
XP_005264935.1:n.*679G>A
|
|
XR_245095.2:n.2811G>A
|
|
|
XM_017005730.1:c.1179G>A
|
XP_016861219.1:p.Leu393=
|
|
XM_024453351.1:c.1560G>A
|
XP_024309119.1:p.Leu520=
|
|
XM_024453352.1:c.*679G>A
|
XP_024309120.1:n.*679G>A
|
|
XR_001740022.2:n.3462G>A
|
|
|
XR_001740023.2:n.2986G>A
|
|
|
XR_245095.4:n.2812G>A
|
|
|
NM_145262.4:c.1560G>A
MANE Select
|
NP_660305.2:p.Leu520=
|
|
NR_026699.2:n.1650G>A
|
|
|
NR_026700.2:n.756G>A
|
|
|
NR_026701.2:n.1648G>A
|
|
|
NR_026702.2:n.686G>A
|
|
|
NM_001144951.2:c.*679G>A
|
NP_001138423.1:n.*679G>A
|
|