ENST00000361337.3:c.1756G>T
(TOP1)
MANE Select
|
ENSP00000354522.2:p.Ala586Ser
|
|
ENST00000680945.1:c.349G>T
(TOP1)
|
ENSP00000504935.1:p.Ala117Ser
|
|
ENST00000681058.1:n.6542G>T
(TOP1)
|
|
|
ENST00000681113.1:c.*1451G>T
(TOP1)
|
ENSP00000505788.1:n.*1451G>T
|
|
ENST00000681392.1:n.3064G>T
(TOP1)
|
|
|
ENST00000681884.1:n.3018G>T
(TOP1)
|
|
|
ENST00000361337.2:c.1756G>T
(TOP1)
|
ENSP00000354522.2:p.Ala586Ser
|
|
NM_003286.2:c.1756G>T
(TOP1)
|
NP_003277.1:p.Ala586Ser
|
|
NR_109889.1:n.711-15037C>A
(PLCG1-AS1)
|
|
|
XM_011529032.1:c.1252G>T
(TOP1)
|
XP_011527334.1:p.Ala418Ser
|
|
XM_011529033.1:c.1018G>T
(TOP1)
|
XP_011527335.1:p.Ala340Ser
|
|
NM_003286.3:c.1756G>T
(TOP1)
|
NP_003277.1:p.Ala586Ser
|
|
NM_003286.4:c.1756G>T
(TOP1)
MANE Select
|
NP_003277.1:p.Ala586Ser
|
|