ENST00000525341.2:c.324A>G
|
|
|
ENST00000528641.7:c.280-704A>G
|
ENSP00000434982.3:n.280-704A>G
|
|
ENST00000529797.2:n.277A>G
|
|
|
ENST00000682324.1:c.347A>G
|
ENSP00000508017.1:p.Glu116Gly
|
|
ENST00000682659.1:c.100-704A>G
|
ENSP00000507351.1:n.100-704A>G
|
|
ENST00000682699.1:c.347A>G
|
ENSP00000507935.1:p.Glu116Gly
|
|
ENST00000683237.1:c.347A>G
|
ENSP00000507343.1:p.Glu116Gly
|
|
ENST00000683856.1:c.170A>G
|
ENSP00000507979.1:p.Glu57Gly
|
|
ENST00000684006.1:c.347A>G
|
ENSP00000507269.1:p.Glu116Gly
|
|
ENST00000684657.1:c.167A>G
|
ENSP00000507961.1:p.Glu56Gly
|
|
ENST00000279146.8:c.347A>G
MANE Select
|
ENSP00000279146.3:p.Glu116Gly
|
|
ENST00000279146.7:c.347A>G
|
ENSP00000279146.3:p.Glu116Gly
|
|
ENST00000528641.6:c.280-704A>G
|
ENSP00000434982.2:n.280-704A>G
|
|
ENST00000529797.1:n.457A>G
|
|
|
NM_001302959.1:c.170A>G
|
NP_001289888.1:p.Glu57Gly
|
|
NM_001302960.1:c.347A>G
|
NP_001289889.1:p.Glu116Gly
|
|
NM_003977.3:c.347A>G
|
NP_003968.3:p.Glu116Gly
|
|
XM_024448761.1:c.347A>G
|
XP_024304529.1:p.Glu116Gly
|
|
NM_003977.4:c.347A>G
MANE Select
|
NP_003968.3:p.Glu116Gly
|
|
NM_001302960.2:c.347A>G
|
NP_001289889.1:p.Glu116Gly
|
|
NM_001302959.2:c.170A>G
|
NP_001289888.1:p.Glu57Gly
|
|