ENST00000471318.6:n.955+376A>G
|
|
|
ENST00000621467.5:c.1033+376A>G
|
ENSP00000480508.2:n.1033+376A>G
|
|
ENST00000686475.1:n.1099+376A>G
|
|
|
ENST00000409883.7:c.1159+376A>G
MANE Select
|
ENSP00000386264.2:n.1159+376A>G
|
|
ENST00000286196.9:c.*723+376A>G
|
ENSP00000286196.5:n.*723+376A>G
|
|
ENST00000409444.6:c.1135+376A>G
|
ENSP00000387203.2:n.1135+376A>G
|
|
ENST00000409883.6:c.1159+376A>G
|
ENSP00000386264.2:n.1159+376A>G
|
|
ENST00000471318.5:n.387+376A>G
|
|
|
ENST00000495329.1:n.298+376A>G
|
|
|
ENST00000621467.4:c.1135+376A>G
|
ENSP00000480508.1:n.1135+376A>G
|
|
NM_001044385.2:c.1159+376A>G
|
NP_001037850.1:n.1159+376A>G
|
|
NM_152388.3:c.1135+376A>G
|
NP_689601.2:n.1135+376A>G
|
|
NM_001044385.3:c.1159+376A>G
MANE Select
|
NP_001037850.1:n.1159+376A>G
|
|
NM_152388.4:c.1135+376A>G
|
NP_689601.2:n.1135+376A>G
|
|