ENST00000527168.6:n.922+1G>T
|
|
|
ENST00000529110.2:c.907+1G>T
|
ENSP00000435349.2:n.907+1G>T
|
|
ENST00000529957.6:n.881+1G>T
|
|
|
ENST00000683366.1:c.*555+1G>T
|
ENSP00000507283.1:n.*555+1G>T
|
|
ENST00000683887.1:c.871+1G>T
|
ENSP00000506886.1:n.871+1G>T
|
|
ENST00000684100.1:n.817+1G>T
|
|
|
ENST00000684126.1:n.957+1G>T
|
|
|
ENST00000684688.1:n.1448+1G>T
|
|
|
ENST00000204679.9:c.823+1G>T
MANE Select
|
ENSP00000204679.4:n.823+1G>T
|
|
ENST00000204679.8:c.823+1G>T
|
ENSP00000204679.4:n.823+1G>T
|
|
ENST00000527076.1:n.2046+1G>T
|
|
|
ENST00000527168.5:n.990+1G>T
|
|
|
NM_032520.4:c.823+1G>T
|
NP_115909.1:n.823+1G>T
|
|
XM_017023782.1:c.871+1G>T
|
XP_016879271.1:n.871+1G>T
|
|
XM_017023783.1:c.463+1G>T
|
XP_016879272.1:n.463+1G>T
|
|
NM_032520.5:c.823+1G>T
MANE Select
|
NP_115909.1:n.823+1G>T
|
|