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NM_013254.4:c.1153G>T
MANE Select
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NP_037386.1:p.Glu385Ter
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ENST00000331710.10:c.1153G>T
MANE Select
|
ENSP00000329967.5:p.Glu385Ter
|
|
NM_013254.3:c.1153G>T
|
NP_037386.1:p.Glu385Ter
|
|
ENST00000331710.9:c.1153G>T
|
ENSP00000329967.5:p.Glu385Ter
|
|
ENST00000536906.1:n.57G>T
|
|
|
ENST00000545025.1:n.423G>T
|
|
|
ENST00000545025.2:c.276G>T
|
|
|
ENST00000650708.1:c.1029G>T
|
|
|
ENST00000650762.1:c.997G>T
|
ENSP00000498758.1:p.Glu333Ter
|
|
ENST00000650786.1:c.*1298G>T
|
ENSP00000498280.1:n.*1298G>T
|
|
ENST00000650790.1:c.1153G>T
|
ENSP00000498995.1:p.Glu385Ter
|
|
ENST00000650997.1:c.1153G>T
|
ENSP00000498341.1:p.Glu385Ter
|
|
ENST00000651014.1:c.997G>T
|
ENSP00000498885.1:p.Glu333Ter
|
|
ENST00000651262.1:c.1153G>T
|
ENSP00000498461.1:p.Glu385Ter
|
|
ENST00000651878.1:c.*637G>T
|
ENSP00000499077.1:n.*637G>T
|
|
ENST00000651889.1:n.904G>T
|
|
|
ENST00000651947.1:n.1241G>T
|
|
|
ENST00000652389.1:c.1153G>T
|
ENSP00000498414.1:p.Glu385Ter
|
|
ENST00000652537.1:c.1153G>T
|
ENSP00000499102.1:p.Glu385Ter
|
|
ENST00000652657.1:c.1153G>T
|
ENSP00000498887.1:p.Glu385Ter
|
|
ENST00000676490.1:c.161G>T
|
|
|
ENST00000676551.1:n.1252G>T
|
|
|
ENST00000676654.1:n.1282G>T
|
|
|
ENST00000676684.1:n.1282G>T
|
|
|
ENST00000676809.1:c.1153G>T
|
ENSP00000504298.1:p.Glu385Ter
|
|
ENST00000676912.1:c.997G>T
|
ENSP00000503567.1:p.Glu333Ter
|
|
ENST00000676930.1:c.992+2442G>T
|
ENSP00000502899.1:n.992+2442G>T
|
|
ENST00000676983.1:c.272G>T
|
|
|
ENST00000677499.1:c.1153G>T
|
ENSP00000502875.1:p.Glu385Ter
|
|
ENST00000677549.1:n.1215G>T
|
|
|
ENST00000677632.1:c.1153G>T
|
ENSP00000504586.1:p.Glu385Ter
|
|
ENST00000677641.1:c.1153G>T
|
ENSP00000504637.1:p.Glu385Ter
|
|
ENST00000677686.1:n.3537G>T
|
|
|
ENST00000677831.1:c.1153G>T
|
ENSP00000503760.1:p.Glu385Ter
|
|
ENST00000677858.1:c.217G>T
|
|
|
ENST00000678180.1:c.1153G>T
|
ENSP00000504132.1:p.Glu385Ter
|
|
ENST00000678197.1:n.1136G>T
|
|
|
XM_005268809.1:c.1153G>T
|
XP_005268866.1:p.Glu385Ter
|
|
XM_005268810.1:c.1153G>T
|
XP_005268867.1:p.Glu385Ter
|
|
XR_001748674.2:n.1267G>T
|
|
|
XR_944524.1:n.1312G>T
|
|
|
XR_944525.1:n.1312G>T
|
|