ENST00000436784.7:c.1518G>T
MANE Select
|
ENSP00000389175.2:p.Gly506=
|
|
ENST00000436784.6:c.1518G>T
|
ENSP00000389175.2:p.Gly506=
|
|
ENST00000461183.5:c.790G>T
|
ENSP00000417264.1:p.Asp264Tyr
|
|
ENST00000471180.5:c.661G>T
|
ENSP00000417526.1:p.Asp221Tyr
|
|
ENST00000473032.5:c.556G>T
|
ENSP00000418951.1:p.Asp186Tyr
|
|
ENST00000486393.5:c.*881G>T
|
ENSP00000419868.1:n.*881G>T
|
|
ENST00000489173.1:n.1812G>T
|
|
|
NM_145262.3:c.1518G>T
|
NP_660305.2:p.Gly506=
|
|
NR_026699.1:n.1616G>T
|
|
|
NR_026700.1:n.722G>T
|
|
|
NR_026701.1:n.1614G>T
|
|
|
NR_026702.1:n.652G>T
|
|
|
XM_005264878.2:c.*637G>T
|
XP_005264935.1:n.*637G>T
|
|
XR_245095.2:n.2769G>T
|
|
|
XM_017005730.1:c.1137G>T
|
XP_016861219.1:p.Gly379=
|
|
XM_024453351.1:c.1518G>T
|
XP_024309119.1:p.Gly506=
|
|
XM_024453352.1:c.*637G>T
|
XP_024309120.1:n.*637G>T
|
|
XR_001740022.2:n.3420G>T
|
|
|
XR_001740023.2:n.2944G>T
|
|
|
XR_245095.4:n.2770G>T
|
|
|
NM_145262.4:c.1518G>T
MANE Select
|
NP_660305.2:p.Gly506=
|
|
NR_026699.2:n.1608G>T
|
|
|
NR_026700.2:n.714G>T
|
|
|
NR_026701.2:n.1606G>T
|
|
|
NR_026702.2:n.644G>T
|
|
|
NM_001144951.2:c.*637G>T
|
NP_001138423.1:n.*637G>T
|
|