ENST00000426263.10:c.972+47G>T
MANE Select
|
ENSP00000416293.2:n.972+47G>T
|
|
ENST00000674545.1:n.337G>T
|
|
|
ENST00000674765.1:c.972+47G>T
|
ENSP00000501811.1:n.972+47G>T
|
|
ENST00000675112.1:n.1273+47G>T
|
|
|
ENST00000676254.1:n.1421+47G>T
|
|
|
ENST00000426263.7:c.972+47G>T
|
ENSP00000416293.2:n.972+47G>T
|
|
ENST00000439722.2:c.851+47G>T
|
ENSP00000395521.2:n.851+47G>T
|
|
ENST00000475162.3:c.415+1463G>T
|
|
|
ENST00000630287.2:c.*287+47G>T
|
ENSP00000486694.1:n.*287+47G>T
|
|
NM_006516.2:c.972+47G>T
|
NP_006507.2:n.972+47G>T
|
|
NM_006516.3:c.972+47G>T
|
NP_006507.2:n.972+47G>T
|
|
NM_006516.4:c.972+47G>T
MANE Select
|
NP_006507.2:n.972+47G>T
|
|