ENST00000570137.7:c.1007+3855T>C
MANE Select
|
ENSP00000476295.1:n.1007+3855T>C
|
|
ENST00000561616.2:n.458+3855T>C
|
|
|
ENST00000562812.5:c.1010+3855T>C
|
ENSP00000454546.1:n.1010+3855T>C
|
|
ENST00000563890.5:c.1010+3855T>C
|
ENSP00000455111.1:n.1010+3855T>C
|
|
ENST00000566173.3:c.1010+3855T>C
|
ENSP00000456934.1:n.1010+3855T>C
|
|
ENST00000570137.6:c.1007+3855T>C
|
ENSP00000476295.1:n.1007+3855T>C
|
|
NM_152342.2:c.1007+3855T>C
|
NP_689555.2:n.1007+3855T>C
|
|
XM_011522866.1:c.1109+3855T>C
|
XP_011521168.1:n.1109+3855T>C
|
|
XM_011522867.1:c.998+3855T>C
|
XP_011521169.1:n.998+3855T>C
|
|
XM_011522868.1:c.830+3855T>C
|
XP_011521170.1:n.830+3855T>C
|
|
NM_152342.3:c.1007+3855T>C
|
NP_689555.2:n.1007+3855T>C
|
|
XM_011522867.2:c.998+3855T>C
|
XP_011521169.1:n.998+3855T>C
|
|
XM_024450151.1:c.830+3855T>C
|
XP_024305919.1:n.830+3855T>C
|
|
NM_152342.4:c.1007+3855T>C
MANE Select
|
NP_689555.2:n.1007+3855T>C
|
|