ENST00000641290.2:n.189+42C>T
|
|
|
ENST00000695905.1:n.312+42C>T
|
|
|
ENST00000695906.1:n.312+42C>T
|
|
|
ENST00000695908.1:n.303+42C>T
|
|
|
ENST00000696169.1:c.184+42C>T
|
ENSP00000512460.1:n.184+42C>T
|
|
ENST00000371732.10:c.184+42C>T
MANE Select
|
ENSP00000360797.5:n.184+42C>T
|
|
ENST00000641290.1:c.-129+42C>T
|
ENSP00000493113.1:n.-129+42C>T
|
|
ENST00000371732.9:c.184+42C>T
|
ENSP00000360797.5:n.184+42C>T
|
|
ENST00000371734.7:c.184+42C>T
|
ENSP00000360799.3:n.184+42C>T
|
|
ENST00000481053.5:n.313+42C>T
|
|
|
ENST00000489932.2:c.184+42C>T
|
ENSP00000451368.1:n.184+42C>T
|
|
ENST00000556340.1:n.315+42C>T
|
|
|
NM_052813.4:c.184+42C>T , LRG_178t1:c.184+42C>T
|
NP_434700.2:n.184+42C>T
|
|
NM_052814.3:c.184+42C>T
|
NP_434701.1:n.184+42C>T
|
|
NM_052813.5:c.184+42C>T
MANE Select
|
NP_434700.2:n.184+42C>T
|
|
NM_052814.4:c.184+42C>T
|
NP_434701.1:n.184+42C>T
|
|