ENST00000527168.6:n.922+17G>C
|
|
|
ENST00000529110.2:c.907+17G>C
|
ENSP00000435349.2:n.907+17G>C
|
|
ENST00000529957.6:n.881+17G>C
|
|
|
ENST00000683366.1:c.*555+17G>C
|
ENSP00000507283.1:n.*555+17G>C
|
|
ENST00000683887.1:c.871+17G>C
|
ENSP00000506886.1:n.871+17G>C
|
|
ENST00000684100.1:n.817+17G>C
|
|
|
ENST00000684126.1:n.957+17G>C
|
|
|
ENST00000684688.1:n.1448+17G>C
|
|
|
ENST00000204679.9:c.823+17G>C
MANE Select
|
ENSP00000204679.4:n.823+17G>C
|
|
ENST00000204679.8:c.823+17G>C
|
ENSP00000204679.4:n.823+17G>C
|
|
ENST00000527076.1:n.2046+17G>C
|
|
|
ENST00000527168.5:n.990+17G>C
|
|
|
NM_032520.4:c.823+17G>C
|
NP_115909.1:n.823+17G>C
|
|
XM_017023782.1:c.871+17G>C
|
XP_016879271.1:n.871+17G>C
|
|
XM_017023783.1:c.463+17G>C
|
XP_016879272.1:n.463+17G>C
|
|
NM_032520.5:c.823+17G>C
MANE Select
|
NP_115909.1:n.823+17G>C
|
|