ENST00000682775.1:c.2185+16545A>T
|
ENSP00000508399.1:n.2185+16545A>T
|
|
ENST00000682944.1:c.6663A>T
|
ENSP00000507173.1:p.Thr2221=
|
|
ENST00000683210.1:c.2185+16545A>T
|
ENSP00000506739.1:n.2185+16545A>T
|
|
ENST00000683270.1:c.6445+182A>T
|
ENSP00000507624.1:n.6445+182A>T
|
|
ENST00000683367.1:c.2177-7756A>T
|
ENSP00000507780.1:n.2177-7756A>T
|
|
ENST00000683489.1:c.2291+4345A>T
|
ENSP00000508403.1:n.2291+4345A>T
|
|
ENST00000683680.1:c.2318+4345A>T
|
ENSP00000507223.1:n.2318+4345A>T
|
|
ENST00000684163.1:c.2204-7756A>T
|
ENSP00000508262.1:n.2204-7756A>T
|
|
ENST00000684196.1:n.4543-7756A>T
|
|
|
ENST00000684325.1:c.2186-15566A>T
|
ENSP00000508121.1:n.2186-15566A>T
|
|
ENST00000684385.1:c.2221-7756A>T
|
ENSP00000507855.1:n.2221-7756A>T
|
|
ENST00000684497.1:c.2186-14596A>T
|
ENSP00000507057.1:n.2186-14596A>T
|
|
ENST00000382292.9:c.6636A>T
MANE Select
|
ENSP00000371729.3:p.Thr2212=
|
|
ENST00000423156.2:c.2186-7756A>T
|
ENSP00000390925.2:n.2186-7756A>T
|
|
ENST00000455470.6:c.2431+4205A>T
|
ENSP00000406565.2:n.2431+4205A>T
|
|
ENST00000382292.7:c.6636A>T
|
ENSP00000371729.3:p.Thr2212=
|
|
ENST00000382298.7:c.6636A>T
|
ENSP00000371735.3:p.Thr2212=
|
|
ENST00000402364.1:c.4386A>T
|
ENSP00000385844.1:p.Thr1462=
|
|
ENST00000423156.1:c.1058-7756A>T
|
ENSP00000390925.1:n.1058-7756A>T
|
|
ENST00000455470.5:c.2129+4205A>T
|
|
|
NM_001278055.1:c.6195A>T
|
NP_001264984.1:p.Thr2065=
|
|
NM_014363.5:c.6636A>T
|
NP_055178.3:p.Thr2212=
|
|
XM_005266338.1:c.6663A>T
|
XP_005266395.1:p.Thr2221=
|
|
XM_011535038.1:c.6687A>T
|
XP_011533340.1:p.Thr2229=
|
|
XM_011535039.1:c.6654A>T
|
XP_011533341.1:p.Thr2218=
|
|
XM_005266338.2:c.6663A>T
|
XP_005266395.1:p.Thr2221=
|
|
XM_011535039.2:c.6654A>T
|
XP_011533341.1:p.Thr2218=
|
|
XM_017020539.1:c.6627A>T
|
XP_016876028.1:p.Thr2209=
|
|
XM_024449337.1:c.6663A>T
|
XP_024305105.1:p.Thr2221=
|
|
NM_014363.6:c.6636A>T
MANE Select
|
NP_055178.3:p.Thr2212=
|
|
NM_001278055.2:c.6195A>T
|
NP_001264984.1:p.Thr2065=
|
|