ENST00000647720.2:c.3517+9A>T
|
ENSP00000497673.2:n.3517+9A>T
|
|
ENST00000647978.2:c.*3240A>T
|
ENSP00000497658.1:n.*3240A>T
|
|
ENST00000649781.2:c.3343A>T
|
ENSP00000497203.1:p.Thr1115Ser
|
|
ENST00000685018.2:c.3526A>T
|
ENSP00000510194.2:p.Thr1176Ser
|
|
ENST00000687278.2:c.*179A>T
|
ENSP00000509593.2:n.*179A>T
|
|
ENST00000699585.1:c.3517+9A>T
|
ENSP00000514456.1:n.3517+9A>T
|
|
ENST00000699598.1:c.3526A>T
|
ENSP00000514467.1:p.Thr1176Ser
|
|
ENST00000699599.1:c.3526A>T
|
ENSP00000514468.1:p.Thr1176Ser
|
|
ENST00000699600.1:c.*187A>T
|
ENSP00000514469.1:n.*187A>T
|
|
ENST00000699601.1:c.*1901A>T
|
ENSP00000514470.1:n.*1901A>T
|
|
ENST00000699602.1:c.3520A>T
|
ENSP00000514471.1:p.Thr1174Ser
|
|
ENST00000699604.1:c.*3350A>T
|
ENSP00000514472.1:n.*3350A>T
|
|
ENST00000699605.1:c.3100A>T
|
ENSP00000514473.1:p.Thr1034Ser
|
|
ENST00000685018.1:c.274A>T
|
ENSP00000510194.1:p.Thr92Ser
|
|
ENST00000687278.1:c.1313A>T
|
ENSP00000509593.1:n.1313A>T
|
|
ENST00000689011.1:c.108A>T
|
|
|
ENST00000003084.11:c.3526A>T
MANE Select
|
ENSP00000003084.6:p.Thr1176Ser
|
|
ENST00000647720.1:c.1167+9A>T
|
|
|
ENST00000648260.1:c.2308A>T
|
ENSP00000497957.1:p.Thr770Ser
|
|
ENST00000649406.1:c.3343A>T
|
ENSP00000497965.1:p.Thr1115Ser
|
|
ENST00000649781.1:c.3343A>T
|
ENSP00000497203.1:p.Thr1115Ser
|
|
ENST00000003084.10:c.3526A>T
|
ENSP00000003084.6:p.Thr1176Ser
|
|
ENST00000426809.5:c.3436A>T
|
ENSP00000389119.1:p.Thr1146Ser
|
|
ENST00000468795.1:c.351A>T
|
|
|
NM_000492.3:c.3526A>T , LRG_663t1:c.3526A>T
|
NP_000483.3:p.Thr1176Ser
|
|
XM_011515751.1:c.3616A>T
|
XP_011514053.1:p.Thr1206Ser
|
|
XM_011515752.1:c.3616A>T
|
XP_011514054.1:p.Thr1206Ser
|
|
XM_011515753.1:c.3283A>T
|
XP_011514055.1:p.Thr1095Ser
|
|
XM_011515754.1:c.3283A>T
|
XP_011514056.1:p.Thr1095Ser
|
|
NM_000492.4:c.3526A>T
MANE Select
|
NP_000483.3:p.Thr1176Ser
|
|