ENST00000703783.1:n.973G>T
|
|
|
ENST00000703785.1:n.1054G>T
|
|
|
ENST00000262464.9:c.4189G>T
MANE Select
|
ENSP00000262464.4:p.Glu1397Ter
|
|
ENST00000262464.8:c.4189G>T
|
ENSP00000262464.4:p.Glu1397Ter
|
|
ENST00000507835.5:c.739G>T
|
ENSP00000426839.1:p.Glu247Ter
|
|
ENST00000508053.5:c.4189G>T
|
ENSP00000424571.1:p.Glu1397Ter
|
|
ENST00000508989.5:c.4090G>T
|
ENSP00000425596.1:p.Glu1364Ter
|
|
ENST00000619499.4:c.4186G>T
|
ENSP00000482132.1:p.Glu1396Ter
|
|
NM_001999.3:c.4189G>T
|
NP_001990.2:p.Glu1397Ter
|
|
XM_017009228.2:c.4036G>T
|
XP_016864717.1:p.Glu1346Ter
|
|
NM_001999.4:c.4189G>T
MANE Select
|
NP_001990.2:p.Glu1397Ter
|
|