ENST00000527168.6:n.510+32G>T
|
|
|
ENST00000529110.2:c.495+32G>T
|
ENSP00000435349.2:n.495+32G>T
|
|
ENST00000529957.6:n.469+32G>T
|
|
|
ENST00000683366.1:c.*143+32G>T
|
ENSP00000507283.1:n.*143+32G>T
|
|
ENST00000683887.1:c.459+32G>T
|
ENSP00000506886.1:n.459+32G>T
|
|
ENST00000684100.1:n.405+32G>T
|
|
|
ENST00000684126.1:n.469+32G>T
|
|
|
ENST00000684688.1:n.1036+32G>T
|
|
|
ENST00000204679.9:c.411+32G>T
MANE Select
|
ENSP00000204679.4:n.411+32G>T
|
|
ENST00000204679.8:c.411+32G>T
|
ENSP00000204679.4:n.411+32G>T
|
|
ENST00000527076.1:n.1427+32G>T
|
|
|
ENST00000527168.5:n.447+32G>T
|
|
|
ENST00000529110.1:c.478+32G>T
|
|
|
ENST00000529957.5:n.510+32G>T
|
|
|
NM_032520.4:c.411+32G>T
|
NP_115909.1:n.411+32G>T
|
|
XM_017023782.1:c.459+32G>T
|
XP_016879271.1:n.459+32G>T
|
|
XM_017023783.1:c.51+32G>T
|
XP_016879272.1:n.51+32G>T
|
|
NM_032520.5:c.411+32G>T
MANE Select
|
NP_115909.1:n.411+32G>T
|
|