ENST00000426263.10:c.1278+15T>G
MANE Select
|
ENSP00000416293.2:n.1278+15T>G
|
|
ENST00000674545.1:n.1895+15T>G
|
|
|
ENST00000674765.1:c.1030-733T>G
|
ENSP00000501811.1:n.1030-733T>G
|
|
ENST00000675112.1:n.1579+15T>G
|
|
|
ENST00000676254.1:n.1727+15T>G
|
|
|
ENST00000426263.7:c.1278+15T>G
|
ENSP00000416293.2:n.1278+15T>G
|
|
ENST00000475162.3:c.416-612T>G
|
|
|
ENST00000630287.2:c.*593+15T>G
|
ENSP00000486694.1:n.*593+15T>G
|
|
NM_006516.2:c.1278+15T>G
|
NP_006507.2:n.1278+15T>G
|
|
NM_006516.3:c.1278+15T>G
|
NP_006507.2:n.1278+15T>G
|
|
NM_006516.4:c.1278+15T>G
MANE Select
|
NP_006507.2:n.1278+15T>G
|
|