ENST00000527168.6:n.708+11G>T
|
|
|
ENST00000529110.2:c.693+11G>T
|
ENSP00000435349.2:n.693+11G>T
|
|
ENST00000529957.6:n.667+11G>T
|
|
|
ENST00000683366.1:c.*341+11G>T
|
ENSP00000507283.1:n.*341+11G>T
|
|
ENST00000683887.1:c.657+11G>T
|
ENSP00000506886.1:n.657+11G>T
|
|
ENST00000684100.1:n.603+11G>T
|
|
|
ENST00000684126.1:n.678G>T
|
|
|
ENST00000684688.1:n.1234+11G>T
|
|
|
ENST00000204679.9:c.609+11G>T
MANE Select
|
ENSP00000204679.4:n.609+11G>T
|
|
ENST00000204679.8:c.609+11G>T
|
ENSP00000204679.4:n.609+11G>T
|
|
ENST00000527076.1:n.1767G>T
|
|
|
ENST00000527168.5:n.776+11G>T
|
|
|
ENST00000529957.5:n.708+11G>T
|
|
|
NM_032520.4:c.609+11G>T
|
NP_115909.1:n.609+11G>T
|
|
XM_017023782.1:c.657+11G>T
|
XP_016879271.1:n.657+11G>T
|
|
XM_017023783.1:c.249+11G>T
|
XP_016879272.1:n.249+11G>T
|
|
NM_032520.5:c.609+11G>T
MANE Select
|
NP_115909.1:n.609+11G>T
|
|