ENST00000405460.9:c.14379A>C
MANE Select
|
ENSP00000384582.2:p.Thr4793=
|
|
ENST00000425867.3:c.3333A>C
|
ENSP00000392618.3:p.Thr1111=
|
|
ENST00000507314.2:c.54A>C
|
ENSP00000491299.1:p.Thr18=
|
|
ENST00000638510.1:n.1646A>C
|
|
|
ENST00000638585.1:n.145A>C
|
|
|
ENST00000638975.1:c.1008A>C
|
ENSP00000492630.1:p.Thr336=
|
|
ENST00000639431.1:c.265+114999A>C
|
ENSP00000491057.1:n.265+114999A>C
|
|
ENST00000640407.1:c.789A>C
|
ENSP00000491425.1:p.Thr263=
|
|
ENST00000405460.6:c.14379A>C
|
ENSP00000384582.2:p.Thr4793=
|
|
ENST00000425867.2:c.1362A>C
|
ENSP00000392618.2:p.Thr454=
|
|
ENST00000507314.1:n.54A>C
|
|
|
NM_032119.3:c.14379A>C
|
NP_115495.3:p.Thr4793=
|
|
NR_003149.1:n.14392A>C
|
|
|
XM_011543675.1:c.14376A>C
|
XP_011541977.1:p.Thr4792=
|
|
XM_011543676.1:c.14298A>C
|
XP_011541978.1:p.Thr4766=
|
|
XM_011543677.1:c.11682A>C
|
XP_011541979.1:p.Thr3894=
|
|
XM_011543678.1:c.14379A>C
|
XP_011541980.1:p.Thr4793=
|
|
NM_032119.4:c.14379A>C
MANE Select
|
NP_115495.3:p.Thr4793=
|
|
XM_017009963.2:c.14400A>C
|
XP_016865452.1:p.Thr4800=
|
|
XM_017009964.2:c.14397A>C
|
XP_016865453.1:p.Thr4799=
|
|
XM_017009965.1:c.14397A>C
|
XP_016865454.1:p.Thr4799=
|
|
XM_017009966.2:c.14319A>C
|
XP_016865455.1:p.Thr4773=
|
|
XM_017009967.1:c.14304A>C
|
XP_016865456.1:p.Thr4768=
|
|
XM_017009968.2:c.14400A>C
|
XP_016865457.1:p.Thr4800=
|
|
XM_017009969.2:c.14400A>C
|
XP_016865458.1:p.Thr4800=
|
|
XM_017009970.2:c.14400A>C
|
XP_016865459.1:p.Thr4800=
|
|
XM_017009971.2:c.14400A>C
|
XP_016865460.1:p.Thr4800=
|
|
XM_017009972.1:c.7518A>C
|
XP_016865461.1:p.Thr2506=
|
|
XM_017009973.1:c.7497A>C
|
XP_016865462.1:p.Thr2499=
|
|
NR_003149.2:n.14395A>C
|
|
|