ENST00000533191.6:c.1290G>T
(TSBP1)
MANE Select
|
ENSP00000431199.1:p.Glu430Asp
|
|
ENST00000375007.8:c.1290G>T
(TSBP1)
|
ENSP00000364146.4:p.Glu430Asp
|
|
ENST00000375015.8:c.1293G>T
(TSBP1)
|
ENSP00000364155.4:p.Glu431Asp
|
|
ENST00000442822.6:c.1269G>T
(TSBP1)
|
ENSP00000411164.2:p.Glu423Asp
|
|
ENST00000447241.6:c.1296G>T
(TSBP1)
|
ENSP00000415517.2:p.Glu432Asp
|
|
ENST00000527965.5:c.1248G>T
(TSBP1)
|
ENSP00000435103.1:p.Glu416Asp
|
|
ENST00000533191.5:c.1290G>T
(TSBP1)
|
ENSP00000431199.1:p.Glu430Asp
|
|
ENST00000612031.4:c.1296G>T
(TSBP1)
|
ENSP00000480403.1:p.Glu432Asp
|
|
ENST00000617061.4:c.1281G>T
(TSBP1)
|
ENSP00000482001.1:p.Glu427Asp
|
|
NM_001286474.1:c.1290G>T
(TSBP1)
|
NP_001273403.1:p.Glu430Asp
|
|
NM_001286475.1:c.1248G>T
(TSBP1)
|
NP_001273404.1:p.Glu416Asp
|
|
NM_006781.4:c.1296G>T
(TSBP1)
|
NP_006772.3:p.Glu432Asp
|
|
XM_011514235.1:c.1350G>T
(TSBP1)
|
XP_011512537.1:p.Glu450Asp
|
|
XM_011514236.1:c.1350G>T
(TSBP1)
|
XP_011512538.1:p.Glu450Asp
|
|
XM_011514237.1:c.1329G>T
(TSBP1)
|
XP_011512539.1:p.Glu443Asp
|
|
XM_011514238.1:c.1326G>T
(TSBP1)
|
XP_011512540.1:p.Glu442Asp
|
|
XM_011514239.1:c.1308G>T
(TSBP1)
|
XP_011512541.1:p.Glu436Asp
|
|
XM_011514240.1:c.1296G>T
(TSBP1)
|
XP_011512542.1:p.Glu432Asp
|
|
XM_011514241.1:c.1293G>T
(TSBP1)
|
XP_011512543.1:p.Glu431Asp
|
|
XM_011514242.1:c.1290G>T
(TSBP1)
|
XP_011512544.1:p.Glu430Asp
|
|
XM_011514243.1:c.1272G>T
(TSBP1)
|
XP_011512545.1:p.Glu424Asp
|
|
XM_011514244.1:c.1269G>T
(TSBP1)
|
XP_011512546.1:p.Glu423Asp
|
|
XM_011514245.1:c.1251G>T
(TSBP1)
|
XP_011512547.1:p.Glu417Asp
|
|
XM_011514246.1:c.1248G>T
(TSBP1)
|
XP_011512548.1:p.Glu416Asp
|
|
XM_011515039.1:c.421+30568C>A
(TSBP1-AS1)
|
XP_011513341.1:n.421+30568C>A
|
|
XM_011515040.1:c.421+30568C>A
(TSBP1-AS1)
|
XP_011513342.1:n.421+30568C>A
|
|
NR_136244.1:n.440+30568C>A
(TSBP1-AS1)
|
|
|
NR_136245.1:n.242+37963C>A
(TSBP1-AS1)
|
|
|
NR_136246.1:n.242+37963C>A
(TSBP1-AS1)
|
|
|
XM_017010182.1:c.1014G>T
(TSBP1)
|
XP_016865671.1:p.Glu338Asp
|
|
XM_024446307.1:c.1428G>T
(TSBP1)
|
XP_024302075.1:p.Glu476Asp
|
|
NM_001286474.2:c.1290G>T
(TSBP1)
MANE Select
|
NP_001273403.1:p.Glu430Asp
|
|
NM_001286475.2:c.1248G>T
(TSBP1)
|
NP_001273404.1:p.Glu416Asp
|
|
NM_006781.5:c.1296G>T
(TSBP1)
|
NP_006772.3:p.Glu432Asp
|
|