NM_001256597.2:c.233+338A>G
MANE Select
|
NP_001243526.1:n.233+338A>G
|
ENST00000522267.6:c.233+338A>G
MANE Select
|
ENSP00000428773.1:n.233+338A>G
|
NM_001007176.4:c.233+338A>G
|
NP_001007177.1:n.233+338A>G
|
NM_001007176.5:c.233+338A>G
|
NP_001007177.1:n.233+338A>G
|
NM_001256596.1:c.233+338A>G
|
NP_001243525.1:n.233+338A>G
|
NM_001256597.1:c.233+338A>G
|
NP_001243526.1:n.233+338A>G
|
NM_001256598.1:c.*140A>G
|
NP_001243527.1:n.*140A>G
|
NM_001256598.2:c.*140A>G
|
NP_001243527.1:n.*140A>G
|
ENST00000303202.8:c.*140A>G
|
ENSP00000304926.8:n.*140A>G
|
ENST00000399653.8:c.233+338A>G
|
ENSP00000382561.4:n.233+338A>G
|
ENST00000517663.5:c.233+338A>G
|
ENSP00000430392.1:n.233+338A>G
|
ENST00000522267.5:c.233+338A>G
|
ENSP00000428773.1:n.233+338A>G
|