ENST00000253122.10:c.1392+16G>A
MANE Select
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ENSP00000253122.5:n.1392+16G>A
|
|
ENST00000253122.9:c.1392+16G>A
|
ENSP00000253122.5:n.1392+16G>A
|
|
ENST00000413787.1:c.321+16G>A
|
ENSP00000400463.1:n.321+16G>A
|
|
ENST00000430077.6:c.1047+16G>A
|
ENSP00000403041.2:n.1047+16G>A
|
|
ENST00000442457.1:c.446+16G>A
|
|
|
ENST00000485324.1:n.1553G>A
|
|
|
NM_001142805.1:c.1362+16G>A
|
NP_001136277.1:n.1362+16G>A
|
|
NM_001142806.1:c.1047+16G>A
|
NP_001136278.1:n.1047+16G>A
|
|
NM_005629.3:c.1392+16G>A
|
NP_005620.1:n.1392+16G>A
|
|
NM_005629.4:c.1392+16G>A
MANE Select
|
NP_005620.1:n.1392+16G>A
|
|
NM_001142805.2:c.1362+16G>A
|
NP_001136277.1:n.1362+16G>A
|
|