ENST00000682892.1:c.-145-11058A>G
|
ENSP00000507214.1:n.-145-11058A>G
|
|
ENST00000303236.9:c.308+2056A>G
MANE Select
|
ENSP00000307235.3:n.308+2056A>G
|
|
ENST00000652099.1:c.306+2056A>G
|
|
|
ENST00000652423.1:c.184+2056A>G
|
ENSP00000498948.1:n.184+2056A>G
|
|
ENST00000652736.1:n.19A>G
|
|
|
ENST00000303236.7:c.308+2056A>G
|
ENSP00000307235.3:n.308+2056A>G
|
|
ENST00000419748.5:c.-311A>G
|
ENSP00000408325.1:n.-311A>G
|
|
NM_001313915.1:c.-311A>G
|
NP_001300844.1:n.-311A>G
|
|
NM_004836.5:c.308+2056A>G
|
NP_004827.4:n.308+2056A>G
|
|
NM_004836.6:c.308+2056A>G
|
NP_004827.4:n.308+2056A>G
|
|
XR_939749.1:n.517+2056A>G
|
|
|
XM_017005376.2:c.-573+2056A>G
|
XP_016860865.1:n.-573+2056A>G
|
|
NM_004836.7:c.308+2056A>G
MANE Select
|
NP_004827.4:n.308+2056A>G
|
|
NM_001313915.2:c.-311A>G
|
NP_001300844.1:n.-311A>G
|
|