ENST00000527168.6:n.784C>G
|
|
|
ENST00000529110.2:c.769C>G
|
ENSP00000435349.2:p.Gln257Glu
|
|
ENST00000529957.6:n.743C>G
|
|
|
ENST00000683366.1:c.*417C>G
|
ENSP00000507283.1:n.*417C>G
|
|
ENST00000683887.1:c.733C>G
|
ENSP00000506886.1:p.Gln245Glu
|
|
ENST00000684100.1:n.679C>G
|
|
|
ENST00000684126.1:n.819C>G
|
|
|
ENST00000684688.1:n.1310C>G
|
|
|
ENST00000204679.9:c.685C>G
MANE Select
|
ENSP00000204679.4:p.Gln229Glu
|
|
ENST00000204679.8:c.685C>G
|
ENSP00000204679.4:p.Gln229Glu
|
|
ENST00000527076.1:n.1908C>G
|
|
|
ENST00000527168.5:n.852C>G
|
|
|
ENST00000529957.5:n.784C>G
|
|
|
NM_032520.4:c.685C>G
|
NP_115909.1:p.Gln229Glu
|
|
XM_017023782.1:c.733C>G
|
XP_016879271.1:p.Gln245Glu
|
|
XM_017023783.1:c.325C>G
|
XP_016879272.1:p.Gln109Glu
|
|
NM_032520.5:c.685C>G
MANE Select
|
NP_115909.1:p.Gln229Glu
|
|