ENST00000703783.1:n.973G>C
|
|
|
ENST00000703785.1:n.1054G>C
|
|
|
ENST00000262464.9:c.4189G>C
MANE Select
|
ENSP00000262464.4:p.Glu1397Gln
|
|
ENST00000262464.8:c.4189G>C
|
ENSP00000262464.4:p.Glu1397Gln
|
|
ENST00000507835.5:c.739G>C
|
ENSP00000426839.1:p.Glu247Gln
|
|
ENST00000508053.5:c.4189G>C
|
ENSP00000424571.1:p.Glu1397Gln
|
|
ENST00000508989.5:c.4090G>C
|
ENSP00000425596.1:p.Glu1364Gln
|
|
ENST00000619499.4:c.4186G>C
|
ENSP00000482132.1:p.Glu1396Gln
|
|
NM_001999.3:c.4189G>C
|
NP_001990.2:p.Glu1397Gln
|
|
XM_017009228.2:c.4036G>C
|
XP_016864717.1:p.Glu1346Gln
|
|
NM_001999.4:c.4189G>C
MANE Select
|
NP_001990.2:p.Glu1397Gln
|
|