ENST00000338468.8:c.1253G>T
|
ENSP00000343589.4:n.1253G>T
|
|
ENST00000366894.6:c.1134G>T
|
ENSP00000355860.2:n.1134G>T
|
|
ENST00000366898.6:c.1375G>T
MANE Select
|
ENSP00000355865.1:p.Gly459Trp
|
|
ENST00000673871.1:c.1456G>T
|
|
|
ENST00000674006.1:n.760G>T
|
|
|
ENST00000674436.1:n.1011G>T
|
|
|
ENST00000338468.7:c.802G>T
|
ENSP00000343589.3:p.Gly268Trp
|
|
ENST00000366894.5:c.802G>T
|
ENSP00000355860.1:p.Gly268Trp
|
|
ENST00000366896.5:c.928G>T
|
ENSP00000355862.1:p.Gly310Trp
|
|
ENST00000366897.5:c.1291G>T
|
ENSP00000355863.1:p.Gly431Trp
|
|
ENST00000366898.5:c.1375G>T
|
ENSP00000355865.1:p.Gly459Trp
|
|
ENST00000479615.5:c.*151G>T
|
ENSP00000434414.1:n.*151G>T
|
|
ENST00000610470.4:c.508G>T
|
ENSP00000483773.1:p.Gly170Trp
|
|
NM_004562.2:c.1375G>T
|
NP_004553.2:p.Gly459Trp
|
|
NM_013987.2:c.1291G>T
|
NP_054642.2:p.Gly431Trp
|
|
NM_013988.2:c.928G>T
|
NP_054643.2:p.Gly310Trp
|
|
XM_011535863.1:c.1372G>T
|
XP_011534165.1:p.Gly458Trp
|
|
XM_017010908.1:c.1489G>T
|
XP_016866397.1:p.Gly497Trp
|
|
XM_017010909.2:c.1135G>T
|
XP_016866398.1:p.Gly379Trp
|
|
XM_024446449.1:c.1138G>T
|
XP_024302217.1:p.Gly380Trp
|
|
XR_001743443.2:n.1567G>T
|
|
|
NM_004562.3:c.1375G>T
MANE Select
|
NP_004553.2:p.Gly459Trp
|
|
NM_013987.3:c.1291G>T
|
NP_054642.2:p.Gly431Trp
|
|
NM_013988.3:c.928G>T
|
NP_054643.2:p.Gly310Trp
|
|