ENST00000253122.10:c.1254+39G>C
MANE Select
|
ENSP00000253122.5:n.1254+39G>C
|
|
ENST00000253122.9:c.1254+39G>C
|
ENSP00000253122.5:n.1254+39G>C
|
|
ENST00000413787.1:c.258-148G>C
|
ENSP00000400463.1:n.258-148G>C
|
|
ENST00000430077.6:c.909+39G>C
|
ENSP00000403041.2:n.909+39G>C
|
|
ENST00000442457.1:c.308+39G>C
|
|
|
ENST00000457723.1:c.238+39G>C
|
ENSP00000394742.1:n.238+39G>C
|
|
ENST00000485324.1:n.1326G>C
|
|
|
NM_001142805.1:c.1224+39G>C
|
NP_001136277.1:n.1224+39G>C
|
|
NM_001142806.1:c.909+39G>C
|
NP_001136278.1:n.909+39G>C
|
|
NM_005629.3:c.1254+39G>C
|
NP_005620.1:n.1254+39G>C
|
|
NM_005629.4:c.1254+39G>C
MANE Select
|
NP_005620.1:n.1254+39G>C
|
|
NM_001142805.2:c.1224+39G>C
|
NP_001136277.1:n.1224+39G>C
|
|