ENST00000614874.2:c.116_118delinsAAG
|
ENSP00000507272.1:p.Glu39=
|
|
ENST00000682620.1:n.1631-870_1631-868delinsAAG
|
|
|
ENST00000684771.1:n.585-870_585-868delinsAAG
|
|
|
ENST00000228872.9:c.116_118delinsAAG
MANE Select
|
ENSP00000228872.4:p.Glu39=
|
|
ENST00000228872.8:c.116_118delinsAAG
|
ENSP00000228872.4:p.Glu39=
|
|
ENST00000396340.1:c.116_118delinsAAG
|
ENSP00000379629.1:p.Glu39=
|
|
ENST00000442489.1:c.95_97delinsAAG
|
ENSP00000407597.1:p.Glu32=
|
|
ENST00000477087.1:n.155-870_155-868delinsAAG
|
|
|
NM_004064.4:c.116_118delinsAAG
|
NP_004055.1:p.Glu39=
|
|
NM_004064.5:c.116_118delinsAAG
MANE Select
|
NP_004055.1:p.Glu39=
|
|