ENST00000322776.11:c.357G>C
MANE Select
|
ENSP00000322450.6:p.Glu119Asp
|
|
ENST00000647561.1:c.357G>C
|
ENSP00000497587.1:p.Glu119Asp
|
|
ENST00000322776.10:c.357G>C
|
ENSP00000322450.6:p.Glu119Asp
|
|
ENST00000415352.6:c.336G>C
|
ENSP00000395368.2:p.Glu112Asp
|
|
ENST00000524838.5:n.414G>C
|
|
|
ENST00000525086.5:n.430G>C
|
|
|
ENST00000526169.1:n.99G>C
|
|
|
ENST00000526770.5:n.216G>C
|
|
|
ENST00000528314.1:c.54G>C
|
ENSP00000434581.1:p.Glu18Asp
|
|
ENST00000528377.1:n.528G>C
|
|
|
ENST00000529867.5:c.321G>C
|
ENSP00000434438.1:p.Glu107Asp
|
|
ENST00000529927.5:c.330G>C
|
ENSP00000436766.1:p.Glu110Asp
|
|
ENST00000530014.5:n.652G>C
|
|
|
ENST00000530103.5:c.*251G>C
|
ENSP00000434575.1:n.*251G>C
|
|
ENST00000530638.1:c.240G>C
|
ENSP00000436936.1:p.Glu80Asp
|
|
ENST00000532244.5:c.54G>C
|
ENSP00000435202.1:p.Glu18Asp
|
|
ENST00000532303.5:c.54G>C
|
ENSP00000432015.1:p.Glu18Asp
|
|
ENST00000532343.5:c.54G>C
|
ENSP00000431751.1:p.Glu18Asp
|
|
ENST00000533075.5:c.336G>C
|
ENSP00000437267.1:p.Glu112Asp
|
|
ENST00000534139.5:n.473G>C
|
|
|
NM_001166102.1:c.330G>C
|
NP_001159574.1:p.Glu110Asp
|
|
NM_007103.3:c.357G>C
|
NP_009034.2:p.Glu119Asp
|
|
NM_001166102.2:c.330G>C
|
NP_001159574.1:p.Glu110Asp
|
|
NM_007103.4:c.357G>C
MANE Select
|
NP_009034.2:p.Glu119Asp
|
|