ENST00000527168.6:n.744T>G
|
|
|
ENST00000529110.2:c.729T>G
|
ENSP00000435349.2:p.Asp243Glu
|
|
ENST00000529957.6:n.703T>G
|
|
|
ENST00000683366.1:c.*377T>G
|
ENSP00000507283.1:n.*377T>G
|
|
ENST00000683887.1:c.693T>G
|
ENSP00000506886.1:p.Asp231Glu
|
|
ENST00000684100.1:n.639T>G
|
|
|
ENST00000684126.1:n.779T>G
|
|
|
ENST00000684688.1:n.1270T>G
|
|
|
ENST00000204679.9:c.645T>G
MANE Select
|
ENSP00000204679.4:p.Asp215Glu
|
|
ENST00000204679.8:c.645T>G
|
ENSP00000204679.4:p.Asp215Glu
|
|
ENST00000527076.1:n.1868T>G
|
|
|
ENST00000527168.5:n.812T>G
|
|
|
ENST00000529957.5:n.744T>G
|
|
|
NM_032520.4:c.645T>G
|
NP_115909.1:p.Asp215Glu
|
|
XM_017023782.1:c.693T>G
|
XP_016879271.1:p.Asp231Glu
|
|
XM_017023783.1:c.285T>G
|
XP_016879272.1:p.Asp95Glu
|
|
NM_032520.5:c.645T>G
MANE Select
|
NP_115909.1:p.Asp215Glu
|
|