|
NM_001745.4:c.633+4A>G
MANE Select
|
NP_001736.1:n.633+4A>G
|
|
ENST00000297156.4:c.633+4A>G
MANE Select
|
ENSP00000297156.2:n.633+4A>G
|
|
NM_001745.3:c.633+4A>G
|
NP_001736.1:n.633+4A>G
|
|
ENST00000297156.3:c.633+4A>G
|
ENSP00000297156.2:n.633+4A>G
|
|
ENST00000514518.1:c.173-2460A>G
|
ENSP00000427331.1:n.173-2460A>G
|
|
ENST00000676819.1:n.3027+4A>G
|
|
|
ENST00000676829.1:c.172+2735A>G
|
ENSP00000503328.1:n.172+2735A>G
|
|
ENST00000677273.1:c.633+4A>G
|
ENSP00000503312.1:n.633+4A>G
|
|
ENST00000677966.1:n.1784A>G
|
|
|
ENST00000678434.1:n.745A>G
|
|
|
ENST00000678771.1:c.630+4A>G
|
ENSP00000504018.1:n.630+4A>G
|
|
XM_011543653.1:c.633+4A>G
|
XP_011541955.1:n.633+4A>G
|