ENST00000699947.1:c.2250+136T>G
|
ENSP00000514703.1:n.2250+136T>G
|
|
ENST00000699948.1:c.*563+136T>G
|
ENSP00000514704.1:n.*563+136T>G
|
|
ENST00000382745.9:c.2250+136T>G
MANE Select
|
ENSP00000372193.4:n.2250+136T>G
|
|
ENST00000262318.12:c.2182+132T>G
|
ENSP00000262318.8:n.2182+132T>G
|
|
ENST00000382745.8:c.2250+136T>G
|
ENSP00000372193.4:n.2250+136T>G
|
|
ENST00000448525.5:c.2178+136T>G
|
ENSP00000410907.1:n.2178+136T>G
|
|
ENST00000563642.6:n.2319+136T>G
|
|
|
ENST00000565092.6:n.1285+136T>G
|
|
|
ENST00000567836.2:n.491+136T>G
|
|
|
NM_001114331.2:c.2178+136T>G
|
NP_001107803.1:n.2178+136T>G
|
|
NM_001287.5:c.2250+136T>G
|
NP_001278.1:n.2250+136T>G
|
|
XM_011522354.1:c.2076+136T>G
|
XP_011520656.1:n.2076+136T>G
|
|
NM_001287.6:c.2250+136T>G
MANE Select
|
NP_001278.1:n.2250+136T>G
|
|
NM_001114331.3:c.2178+136T>G
|
NP_001107803.1:n.2178+136T>G
|
|