|
ENST00000682775.1:c.2185+17373A>T
|
ENSP00000508399.1:n.2185+17373A>T
|
|
|
ENST00000682944.1:c.7491A>T
|
ENSP00000507173.1:p.Ile2497=
|
|
|
ENST00000683210.1:c.2185+17373A>T
|
ENSP00000506739.1:n.2185+17373A>T
|
|
|
ENST00000683270.1:c.6445+1010A>T
|
ENSP00000507624.1:n.6445+1010A>T
|
|
|
ENST00000683367.1:c.2177-6928A>T
|
ENSP00000507780.1:n.2177-6928A>T
|
|
|
ENST00000683489.1:c.2291+5173A>T
|
ENSP00000508403.1:n.2291+5173A>T
|
|
|
ENST00000683680.1:c.2318+5173A>T
|
ENSP00000507223.1:n.2318+5173A>T
|
|
|
ENST00000684163.1:c.2204-6928A>T
|
ENSP00000508262.1:n.2204-6928A>T
|
|
|
ENST00000684196.1:n.4543-6928A>T
|
|
|
|
ENST00000684325.1:c.2186-14738A>T
|
ENSP00000508121.1:n.2186-14738A>T
|
|
|
ENST00000684385.1:c.2221-6928A>T
|
ENSP00000507855.1:n.2221-6928A>T
|
|
|
ENST00000684497.1:c.2186-13768A>T
|
ENSP00000507057.1:n.2186-13768A>T
|
|
|
ENST00000382292.9:c.7464A>T
MANE Select
|
ENSP00000371729.3:p.Ile2488=
|
|
|
ENST00000423156.2:c.2186-6928A>T
|
ENSP00000390925.2:n.2186-6928A>T
|
|
|
ENST00000455470.6:c.2431+5033A>T
|
ENSP00000406565.2:n.2431+5033A>T
|
|
|
ENST00000382292.7:c.7464A>T
|
ENSP00000371729.3:p.Ile2488=
|
|
|
ENST00000382298.7:c.7464A>T
|
ENSP00000371735.3:p.Ile2488=
|
|
|
ENST00000402364.1:c.5214A>T
|
ENSP00000385844.1:p.Ile1738=
|
|
|
ENST00000423156.1:c.1058-6928A>T
|
ENSP00000390925.1:n.1058-6928A>T
|
|
|
ENST00000455470.5:c.2129+5033A>T
|
|
|
|
NM_001278055.1:c.7023A>T
|
NP_001264984.1:p.Ile2341=
|
|
|
NM_014363.5:c.7464A>T
|
NP_055178.3:p.Ile2488=
|
|
|
XM_005266338.1:c.7491A>T
|
XP_005266395.1:p.Ile2497=
|
|
|
XM_011535038.1:c.7515A>T
|
XP_011533340.1:p.Ile2505=
|
|
|
XM_011535039.1:c.7482A>T
|
XP_011533341.1:p.Ile2494=
|
|
|
XM_005266338.2:c.7491A>T
|
XP_005266395.1:p.Ile2497=
|
|
|
XM_011535039.2:c.7482A>T
|
XP_011533341.1:p.Ile2494=
|
|
|
XM_017020539.1:c.7455A>T
|
XP_016876028.1:p.Ile2485=
|
|
|
XM_024449337.1:c.7491A>T
|
XP_024305105.1:p.Ile2497=
|
|
|
NM_014363.6:c.7464A>T
MANE Select
|
NP_055178.3:p.Ile2488=
|
|
|
NM_001278055.2:c.7023A>T
|
NP_001264984.1:p.Ile2341=
|
|
