ENST00000436784.7:c.457C>T
MANE Select
|
ENSP00000389175.2:p.Arg153Trp
|
|
ENST00000305690.12:c.457C>T
|
ENSP00000301965.9:p.Arg153Trp
|
|
ENST00000436784.6:c.457C>T
|
ENSP00000389175.2:p.Arg153Trp
|
|
ENST00000461183.5:c.205C>T
|
ENSP00000417264.1:p.Arg69Trp
|
|
ENST00000471180.5:c.76C>T
|
ENSP00000417526.1:p.Arg26Trp
|
|
ENST00000473032.5:c.457C>T
|
ENSP00000418951.1:p.Arg153Trp
|
|
ENST00000473583.1:n.726C>T
|
|
|
ENST00000477382.1:c.457C>T
|
ENSP00000419008.1:p.Arg153Trp
|
|
ENST00000486393.5:c.457C>T
|
ENSP00000419868.1:p.Arg153Trp
|
|
ENST00000489173.1:n.116C>T
|
|
|
NM_001144951.1:c.457C>T
|
NP_001138423.1:p.Arg153Trp
|
|
NM_145262.3:c.457C>T
|
NP_660305.2:p.Arg153Trp
|
|
NR_026699.1:n.553C>T
|
|
|
NR_026700.1:n.137C>T
|
|
|
NR_026701.1:n.553C>T
|
|
|
NR_026702.1:n.553C>T
|
|
|
XM_005264878.2:c.457C>T
|
XP_005264935.1:p.Arg153Trp
|
|
XR_245095.2:n.2360C>T
|
|
|
XM_017005730.1:c.76C>T
|
XP_016861219.1:p.Arg26Trp
|
|
XM_024453351.1:c.457C>T
|
XP_024309119.1:p.Arg153Trp
|
|
XM_024453352.1:c.457C>T
|
XP_024309120.1:p.Arg153Trp
|
|
XR_001740022.2:n.2359C>T
|
|
|
XR_001740023.2:n.2359C>T
|
|
|
XR_245095.4:n.2361C>T
|
|
|
NM_145262.4:c.457C>T
MANE Select
|
NP_660305.2:p.Arg153Trp
|
|
NR_026699.2:n.545C>T
|
|
|
NR_026700.2:n.129C>T
|
|
|
NR_026701.2:n.545C>T
|
|
|
NR_026702.2:n.545C>T
|
|
|
NM_001144951.2:c.457C>T
|
NP_001138423.1:p.Arg153Trp
|
|