ENST00000527168.6:n.895C>G
|
|
|
ENST00000529110.2:c.880C>G
|
ENSP00000435349.2:p.His294Asp
|
|
ENST00000529957.6:n.854C>G
|
|
|
ENST00000683366.1:c.*528C>G
|
ENSP00000507283.1:n.*528C>G
|
|
ENST00000683887.1:c.844C>G
|
ENSP00000506886.1:p.His282Asp
|
|
ENST00000684100.1:n.790C>G
|
|
|
ENST00000684126.1:n.930C>G
|
|
|
ENST00000684688.1:n.1421C>G
|
|
|
ENST00000204679.9:c.796C>G
MANE Select
|
ENSP00000204679.4:p.His266Asp
|
|
ENST00000204679.8:c.796C>G
|
ENSP00000204679.4:p.His266Asp
|
|
ENST00000527076.1:n.2019C>G
|
|
|
ENST00000527168.5:n.963C>G
|
|
|
ENST00000529957.5:n.895C>G
|
|
|
NM_032520.4:c.796C>G
|
NP_115909.1:p.His266Asp
|
|
XM_017023782.1:c.844C>G
|
XP_016879271.1:p.His282Asp
|
|
XM_017023783.1:c.436C>G
|
XP_016879272.1:p.His146Asp
|
|
NM_032520.5:c.796C>G
MANE Select
|
NP_115909.1:p.His266Asp
|
|