ENST00000527168.6:n.547C>G
|
|
|
ENST00000529110.2:c.532C>G
|
ENSP00000435349.2:p.His178Asp
|
|
ENST00000529957.6:n.506C>G
|
|
|
ENST00000683366.1:c.*180C>G
|
ENSP00000507283.1:n.*180C>G
|
|
ENST00000683887.1:c.496C>G
|
ENSP00000506886.1:p.His166Asp
|
|
ENST00000684100.1:n.442C>G
|
|
|
ENST00000684126.1:n.506C>G
|
|
|
ENST00000684688.1:n.1073C>G
|
|
|
ENST00000204679.9:c.448C>G
MANE Select
|
ENSP00000204679.4:p.His150Asp
|
|
ENST00000204679.8:c.448C>G
|
ENSP00000204679.4:p.His150Asp
|
|
ENST00000527076.1:n.1464C>G
|
|
|
ENST00000527168.5:n.484C>G
|
|
|
ENST00000529110.1:c.515C>G
|
|
|
ENST00000529957.5:n.547C>G
|
|
|
NM_032520.4:c.448C>G
|
NP_115909.1:p.His150Asp
|
|
XM_017023782.1:c.496C>G
|
XP_016879271.1:p.His166Asp
|
|
XM_017023783.1:c.88C>G
|
XP_016879272.1:p.His30Asp
|
|
NM_032520.5:c.448C>G
MANE Select
|
NP_115909.1:p.His150Asp
|
|