ENST00000356392.9:c.1277+9C>A
MANE Select
|
ENSP00000348757.3:n.1277+9C>A
|
|
ENST00000356392.8:c.1277+9C>A
|
ENSP00000348757.3:n.1277+9C>A
|
|
ENST00000586836.5:c.704+9C>A
|
ENSP00000467429.1:n.704+9C>A
|
|
ENST00000591179.5:c.1097+9C>A
|
ENSP00000466800.1:n.1097+9C>A
|
|
ENST00000591345.5:c.*1196+9C>A
|
ENSP00000467313.1:n.*1196+9C>A
|
|
NM_001302453.1:c.1115+9C>A
|
NP_001289382.1:n.1115+9C>A
|
|
NM_001302454.1:c.1097+9C>A
|
NP_001289383.1:n.1097+9C>A
|
|
NM_145045.4:c.1277+9C>A
|
NP_659482.3:n.1277+9C>A
|
|
NM_145045.5:c.1277+9C>A
MANE Select
|
NP_659482.3:n.1277+9C>A
|
|
NM_001302454.2:c.1097+9C>A
|
NP_001289383.1:n.1097+9C>A
|
|