|
ENST00000682775.1:c.2185+15360G>T
|
ENSP00000508399.1:n.2185+15360G>T
|
|
|
ENST00000682944.1:c.5478G>T
|
ENSP00000507173.1:p.Thr1826=
|
|
|
ENST00000683210.1:c.2185+15360G>T
|
ENSP00000506739.1:n.2185+15360G>T
|
|
|
ENST00000683270.1:c.5442G>T
|
ENSP00000507624.1:p.Thr1814=
|
|
|
ENST00000683367.1:c.2177-8941G>T
|
ENSP00000507780.1:n.2177-8941G>T
|
|
|
ENST00000683489.1:c.2291+3160G>T
|
ENSP00000508403.1:n.2291+3160G>T
|
|
|
ENST00000683680.1:c.2318+3160G>T
|
ENSP00000507223.1:n.2318+3160G>T
|
|
|
ENST00000684163.1:c.2203+8386G>T
|
ENSP00000508262.1:n.2203+8386G>T
|
|
|
ENST00000684196.1:n.4543-8941G>T
|
|
|
|
ENST00000684325.1:c.2185+15360G>T
|
ENSP00000508121.1:n.2185+15360G>T
|
|
|
ENST00000684385.1:c.2220+8386G>T
|
ENSP00000507855.1:n.2220+8386G>T
|
|
|
ENST00000684497.1:c.2185+15360G>T
|
ENSP00000507057.1:n.2185+15360G>T
|
|
|
ENST00000382292.9:c.5451G>T
MANE Select
|
ENSP00000371729.3:p.Thr1817=
|
|
|
ENST00000423156.2:c.2186-8941G>T
|
ENSP00000390925.2:n.2186-8941G>T
|
|
|
ENST00000455470.6:c.2431+3020G>T
|
ENSP00000406565.2:n.2431+3020G>T
|
|
|
ENST00000382292.7:c.5451G>T
|
ENSP00000371729.3:p.Thr1817=
|
|
|
ENST00000382298.7:c.5451G>T
|
ENSP00000371735.3:p.Thr1817=
|
|
|
ENST00000402364.1:c.3201G>T
|
ENSP00000385844.1:p.Thr1067=
|
|
|
ENST00000423156.1:c.1058-8941G>T
|
ENSP00000390925.1:n.1058-8941G>T
|
|
|
ENST00000455470.5:c.2129+3020G>T
|
|
|
|
NM_001278055.1:c.5010G>T
|
NP_001264984.1:p.Thr1670=
|
|
|
NM_014363.5:c.5451G>T
|
NP_055178.3:p.Thr1817=
|
|
|
XM_005266338.1:c.5478G>T
|
XP_005266395.1:p.Thr1826=
|
|
|
XM_011535038.1:c.5502G>T
|
XP_011533340.1:p.Thr1834=
|
|
|
XM_011535039.1:c.5469G>T
|
XP_011533341.1:p.Thr1823=
|
|
|
XM_005266338.2:c.5478G>T
|
XP_005266395.1:p.Thr1826=
|
|
|
XM_011535039.2:c.5469G>T
|
XP_011533341.1:p.Thr1823=
|
|
|
XM_017020539.1:c.5442G>T
|
XP_016876028.1:p.Thr1814=
|
|
|
XM_024449337.1:c.5478G>T
|
XP_024305105.1:p.Thr1826=
|
|
|
NM_014363.6:c.5451G>T
MANE Select
|
NP_055178.3:p.Thr1817=
|
|
|
NM_001278055.2:c.5010G>T
|
NP_001264984.1:p.Thr1670=
|
|
