|
NM_006767.4:c.1615+2T>C
MANE Select
|
NP_006758.2:n.1615+2T>C
|
|
ENST00000646124.2:c.1615+2T>C
MANE Select
|
ENSP00000496779.1:n.1615+2T>C
|
|
NM_006767.3:c.1615+2T>C
|
NP_006758.2:n.1615+2T>C
|
|
ENST00000215739.12:c.1615+2T>C
|
ENSP00000215739.8:n.1615+2T>C
|
|
ENST00000415354.6:c.43+2T>C
|
ENSP00000393765.2:n.43+2T>C
|
|
ENST00000479606.5:n.1761+2T>C
|
|
|
ENST00000492480.1:n.666T>C
|
|
|
ENST00000495142.6:n.962T>C
|
|
|
ENST00000642151.1:c.1446+2T>C
|
|
|
ENST00000643578.1:n.1637+2T>C
|
|
|
ENST00000643710.1:n.476+2T>C
|
|
|
ENST00000646506.1:n.1196T>C
|
|
|
ENST00000700578.1:c.1615+2T>C
|
ENSP00000515073.1:n.1615+2T>C
|