ENST00000403733.8:c.3376G>T
MANE Select
|
ENSP00000384222.3:p.Glu1126Ter
|
|
ENST00000403733.7:c.3376G>T
|
ENSP00000384222.3:p.Glu1126Ter
|
|
ENST00000427431.5:c.*2768G>T
|
ENSP00000393342.1:n.*2768G>T
|
|
ENST00000438543.5:c.*1172G>T
|
ENSP00000413521.1:n.*1172G>T
|
|
ENST00000448232.6:c.3448G>T
|
ENSP00000398577.2:p.Glu1150Ter
|
|
ENST00000504005.5:c.2422G>T
|
ENSP00000427569.1:p.Glu808Ter
|
|
ENST00000508747.1:c.760G>T
|
ENSP00000420835.1:p.Glu254Ter
|
|
ENST00000513834.5:c.3229G>T
|
ENSP00000425054.1:p.Glu1077Ter
|
|
NM_024949.5:c.3376G>T
|
NP_079225.5:p.Glu1126Ter
|
|
XM_011532269.1:c.3448G>T
|
XP_011530571.1:p.Glu1150Ter
|
|
XM_011532269.3:c.3448G>T
|
XP_011530571.1:p.Glu1150Ter
|
|
XM_024454225.1:c.3154G>T
|
XP_024309993.1:p.Glu1052Ter
|
|
NM_024949.6:c.3376G>T
MANE Select
|
NP_079225.5:p.Glu1126Ter
|
|