|
NM_001002294.3:c.1231G>T
MANE Select
|
NP_001002294.1:p.Glu411Ter
|
|
ENST00000367755.9:c.1231G>T
MANE Select
|
ENSP00000356729.4:p.Glu411Ter
|
|
NM_001002294.2:c.1231G>T
|
NP_001002294.1:p.Glu411Ter
|
|
NM_001319173.1:c.1171G>T
|
NP_001306102.1:p.Glu391Ter
|
|
NM_001319173.2:c.1171G>T
|
NP_001306102.1:p.Glu391Ter
|
|
NM_001319174.1:c.1042G>T
|
NP_001306103.1:p.Glu348Ter
|
|
NM_001319174.2:c.1042G>T
|
NP_001306103.1:p.Glu348Ter
|
|
NM_006894.5:c.1231G>T
|
NP_008825.4:p.Glu411Ter
|
|
NM_006894.6:c.1231G>T
|
NP_008825.4:p.Glu411Ter
|
|
ENST00000367755.8:c.1231G>T
|
ENSP00000356729.4:p.Glu411Ter
|
|
XM_005245044.1:c.1042G>T
|
XP_005245101.1:p.Glu348Ter
|
|
XM_011509345.1:c.1171G>T
|
XP_011507647.1:p.Glu391Ter
|
|
XM_011509345.3:c.1171G>T
|
XP_011507647.1:p.Glu391Ter
|
|
XM_011509346.1:c.1171G>T
|
XP_011507648.1:p.Glu391Ter
|
|
XM_024454365.1:c.484G>T
|
XP_024310133.1:p.Glu162Ter
|