ENST00000426263.10:c.867+27T>G
MANE Select
|
ENSP00000416293.2:n.867+27T>G
|
|
ENST00000674765.1:c.867+27T>G
|
ENSP00000501811.1:n.867+27T>G
|
|
ENST00000675112.1:n.917T>G
|
|
|
ENST00000676254.1:n.1316+27T>G
|
|
|
ENST00000426263.7:c.867+27T>G
|
ENSP00000416293.2:n.867+27T>G
|
|
ENST00000439722.2:c.746+27T>G
|
ENSP00000395521.2:n.746+27T>G
|
|
ENST00000475162.3:c.415+1060T>G
|
|
|
ENST00000630287.2:c.*182+27T>G
|
ENSP00000486694.1:n.*182+27T>G
|
|
NM_006516.2:c.867+27T>G
|
NP_006507.2:n.867+27T>G
|
|
NM_006516.3:c.867+27T>G
|
NP_006507.2:n.867+27T>G
|
|
NM_006516.4:c.867+27T>G
MANE Select
|
NP_006507.2:n.867+27T>G
|
|