ENST00000703783.1:n.578A>G
|
|
|
ENST00000703785.1:n.659A>G
|
|
|
ENST00000262464.9:c.3794A>G
MANE Select
|
ENSP00000262464.4:p.Glu1265Gly
|
|
ENST00000262464.8:c.3794A>G
|
ENSP00000262464.4:p.Glu1265Gly
|
|
ENST00000507835.5:c.344A>G
|
ENSP00000426839.1:p.Glu115Gly
|
|
ENST00000508053.5:c.3794A>G
|
ENSP00000424571.1:p.Glu1265Gly
|
|
ENST00000508989.5:c.3695A>G
|
ENSP00000425596.1:p.Glu1232Gly
|
|
ENST00000619499.4:c.3791A>G
|
ENSP00000482132.1:p.Glu1264Gly
|
|
NM_001999.3:c.3794A>G
|
NP_001990.2:p.Glu1265Gly
|
|
XM_017009228.2:c.3641A>G
|
XP_016864717.1:p.Glu1214Gly
|
|
NM_001999.4:c.3794A>G
MANE Select
|
NP_001990.2:p.Glu1265Gly
|
|