ENST00000261304.7:c.420G>T
MANE Select
|
ENSP00000261304.2:p.Arg140Ser
|
|
ENST00000261304.6:c.420G>T
|
ENSP00000261304.2:p.Arg140Ser
|
|
ENST00000393568.8:c.351G>T
|
ENSP00000377198.4:p.Arg117Ser
|
|
ENST00000393569.6:c.342G>T
|
ENSP00000377199.2:p.Arg114Ser
|
|
ENST00000474294.6:n.410G>T
|
|
|
ENST00000544807.6:c.252G>T
|
ENSP00000437513.2:p.Arg84Ser
|
|
ENST00000554372.5:c.*169G>T
|
ENSP00000451884.1:n.*169G>T
|
|
ENST00000554916.5:n.299G>T
|
|
|
ENST00000556261.5:n.121G>T
|
|
|
ENST00000556879.5:c.480G>T
|
ENSP00000452208.1:n.480G>T
|
|
ENST00000557316.5:c.420G>T
|
ENSP00000452314.1:p.Arg140Ser
|
|
ENST00000622264.4:c.410G>T
|
|
|
NM_000153.3:c.420G>T
|
NP_000144.2:p.Arg140Ser
|
|
NM_001201401.1:c.351G>T
|
NP_001188330.1:p.Arg117Ser
|
|
NM_001201402.1:c.342G>T
|
NP_001188331.1:p.Arg114Ser
|
|
XM_011536618.1:c.252G>T
|
XP_011534920.1:p.Arg84Ser
|
|
XM_011536618.2:c.252G>T
|
XP_011534920.1:p.Arg84Ser
|
|
NM_000153.4:c.420G>T
MANE Select
|
NP_000144.2:p.Arg140Ser
|
|
NM_001201401.2:c.351G>T
|
NP_001188330.1:p.Arg117Ser
|
|
NM_001201402.2:c.342G>T
|
NP_001188331.1:p.Arg114Ser
|
|