ENST00000426263.10:c.114+114T>G
MANE Select
|
ENSP00000416293.2:n.114+114T>G
|
|
ENST00000674765.1:c.114+114T>G
|
ENSP00000501811.1:n.114+114T>G
|
|
ENST00000675112.1:n.137+114T>G
|
|
|
ENST00000372500.4:c.19-11906T>G
|
ENSP00000361578.4:n.19-11906T>G
|
|
ENST00000415851.6:n.331+114T>G
|
|
|
ENST00000426263.7:c.114+114T>G
|
ENSP00000416293.2:n.114+114T>G
|
|
ENST00000475162.3:c.13+114T>G
|
|
|
ENST00000625233.2:n.322+114T>G
|
|
|
ENST00000628173.1:n.333+114T>G
|
|
|
ENST00000630287.2:c.114+114T>G
|
ENSP00000486694.1:n.114+114T>G
|
|
ENST00000630821.1:n.445T>G
|
|
|
NM_006516.2:c.114+114T>G
|
NP_006507.2:n.114+114T>G
|
|
NM_006516.3:c.114+114T>G
|
NP_006507.2:n.114+114T>G
|
|
NM_006516.4:c.114+114T>G
MANE Select
|
NP_006507.2:n.114+114T>G
|
|