ENST00000703783.1:n.900A>G
|
|
|
ENST00000703785.1:n.981A>G
|
|
|
ENST00000262464.9:c.4116A>G
MANE Select
|
ENSP00000262464.4:p.Glu1372=
|
|
ENST00000262464.8:c.4116A>G
|
ENSP00000262464.4:p.Glu1372=
|
|
ENST00000507835.5:c.666A>G
|
ENSP00000426839.1:p.Glu222=
|
|
ENST00000508053.5:c.4116A>G
|
ENSP00000424571.1:p.Glu1372=
|
|
ENST00000508989.5:c.4017A>G
|
ENSP00000425596.1:p.Glu1339=
|
|
ENST00000619499.4:c.4113A>G
|
ENSP00000482132.1:p.Glu1371=
|
|
NM_001999.3:c.4116A>G
|
NP_001990.2:p.Glu1372=
|
|
XM_017009228.2:c.3963A>G
|
XP_016864717.1:p.Glu1321=
|
|
NM_001999.4:c.4116A>G
MANE Select
|
NP_001990.2:p.Glu1372=
|
|