ENST00000322344.8:c.1126+14T>G
MANE Select
|
ENSP00000323511.2:n.1126+14T>G
|
|
ENST00000322344.7:c.1126+14T>G
|
ENSP00000323511.2:n.1126+14T>G
|
|
ENST00000593706.3:n.495T>G
|
|
|
ENST00000593946.5:c.*1053+14T>G
|
ENSP00000468896.1:n.*1053+14T>G
|
|
ENST00000594661.5:n.1627+14T>G
|
|
|
ENST00000596014.5:c.1126+14T>G
|
ENSP00000472300.1:n.1126+14T>G
|
|
ENST00000600573.5:c.1033+14T>G
|
ENSP00000469826.1:n.1033+14T>G
|
|
ENST00000600910.5:c.1126+14T>G
|
ENSP00000473137.1:n.1126+14T>G
|
|
ENST00000601816.3:n.25+14T>G
|
|
|
ENST00000625216.2:c.208-66T>G
|
ENSP00000486898.1:n.208-66T>G
|
|
ENST00000627232.2:c.1046+14T>G
|
ENSP00000486037.1:n.1046+14T>G
|
|
ENST00000627317.1:c.747+14T>G
|
|
|
ENST00000631020.2:c.1018+14T>G
|
ENSP00000486707.1:n.1018+14T>G
|
|
NM_007254.3:c.1126+14T>G
|
NP_009185.2:n.1126+14T>G
|
|
NM_007254.4:c.1126+14T>G
MANE Select
|
NP_009185.2:n.1126+14T>G
|
|