|
ENST00000355699.7:c.2281G=
MANE Select
|
ENSP00000347927.2:p.Gly761=
|
|
|
ENST00000355699.6:c.2281G=
|
ENSP00000347927.2:p.Gly761=
|
|
|
ENST00000356589.6:c.2188G=
|
ENSP00000348997.2:p.Gly730=
|
|
|
ENST00000371916.5:c.1225-1441G=
|
ENSP00000360984.2:n.1225-1441G=
|
|
|
ENST00000371929.7:c.2281G=
|
ENSP00000360997.3:p.Gly761=
|
|
|
ENST00000474918.1:c.*819G=
|
ENSP00000435305.1:n.*819G=
|
|
|
ENST00000485925.5:n.1237-1441G=
|
|
|
|
ENST00000495234.5:c.*1253-1441G=
|
ENSP00000435274.1:n.*1253-1441G=
|
|
|
NM_139025.4:c.2281G= , LRG_544t1:c.2281G=
|
NP_620594.1:p.Gly761=
|
|
|
NM_139026.4:c.2188G=
|
NP_620595.1:p.Gly730=
|
|
|
NM_139027.4:c.2281G=
|
NP_620596.2:p.Gly761=
|
|
|
NR_024514.2:n.1256-1441G=
|
|
|
|
XM_011518174.1:c.1891G=
|
XP_011516476.1:p.Gly631=
|
|
|
XM_011518175.1:c.2281G=
|
XP_011516477.1:p.Gly761=
|
|
|
XM_011518176.1:c.1297G=
|
XP_011516478.1:p.Gly433=
|
|
|
XM_011518177.1:c.1291G=
|
XP_011516479.1:p.Gly431=
|
|
|
XM_011518178.1:c.946G=
|
XP_011516480.1:p.Gly316=
|
|
|
XM_011518179.1:c.946G=
|
XP_011516481.1:p.Gly316=
|
|
|
XM_011518180.1:c.687-1441G=
|
XP_011516482.1:n.687-1441G=
|
|
|
XM_011518176.3:c.1297G=
|
XP_011516478.1:p.Gly433=
|
|
|
XM_011518178.2:c.946G=
|
XP_011516480.1:p.Gly316=
|
|
|
XM_017014232.1:c.2269G=
|
XP_016869721.1:p.Gly757=
|
|
|
XM_017014233.1:c.1891G=
|
XP_016869722.1:p.Gly631=
|
|
|
XM_017014234.2:c.1291G=
|
XP_016869723.1:p.Gly431=
|
|
|
XM_017014235.1:c.2234+679G=
|
XP_016869724.1:n.2234+679G=
|
|
|
XR_001746171.1:n.3194-1441G=
|
|
|
|
NM_139026.5:c.2188G=
|
NP_620595.1:p.Gly730=
|
|
|
NM_139027.5:c.2281G=
|
NP_620596.2:p.Gly761=
|
|
|
NM_139025.5:c.2281G=
|
NP_620594.1:p.Gly761=
|
|
|
NM_139026.6:c.2188G=
|
NP_620595.1:p.Gly730=
|
|
|
NM_139027.6:c.2281G=
MANE Select
|
NP_620596.2:p.Gly761=
|
|
|
NR_024514.3:n.1258-1441G=
|
|
|
