ENST00000527168.6:n.332+9A>G
|
|
|
ENST00000529110.2:c.317+9A>G
|
ENSP00000435349.2:n.317+9A>G
|
|
ENST00000529957.6:n.291+9A>G
|
|
|
ENST00000683366.1:c.179-66A>G
|
ENSP00000507283.1:n.179-66A>G
|
|
ENST00000683887.1:c.281+9A>G
|
ENSP00000506886.1:n.281+9A>G
|
|
ENST00000684100.1:n.162A>G
|
|
|
ENST00000684126.1:n.291+9A>G
|
|
|
ENST00000684688.1:n.858+9A>G
|
|
|
ENST00000204679.9:c.233+9A>G
MANE Select
|
ENSP00000204679.4:n.233+9A>G
|
|
ENST00000204679.8:c.233+9A>G
|
ENSP00000204679.4:n.233+9A>G
|
|
ENST00000526820.5:c.*135+9A>G
|
ENSP00000434413.1:n.*135+9A>G
|
|
ENST00000527076.1:n.1184A>G
|
|
|
ENST00000527168.5:n.270-66A>G
|
|
|
ENST00000529110.1:c.300+9A>G
|
|
|
ENST00000529957.5:n.332+9A>G
|
|
|
NM_032520.4:c.233+9A>G
|
NP_115909.1:n.233+9A>G
|
|
XM_017023782.1:c.281+9A>G
|
XP_016879271.1:n.281+9A>G
|
|
XM_017023783.1:c.-128+9A>G
|
XP_016879272.1:n.-128+9A>G
|
|
NM_032520.5:c.233+9A>G
MANE Select
|
NP_115909.1:n.233+9A>G
|
|