ENST00000358823.7:c.4131+162G=
MANE Select
|
ENSP00000351684.2:n.4131+162G=
|
|
ENST00000236925.8:c.4164+162G=
|
ENSP00000236925.4:n.4164+162G=
|
|
ENST00000358823.6:c.4131+162G=
|
ENSP00000351684.2:n.4131+162G=
|
|
ENST00000413307.6:c.4083+162G=
|
ENSP00000416800.2:n.4083+162G=
|
|
ENST00000475326.1:c.313G=
|
|
|
NM_001297707.1:c.4164+162G=
|
NP_001284636.1:n.4164+162G=
|
|
NM_001297708.1:c.4083+162G=
|
NP_001284637.1:n.4083+162G=
|
|
NM_203459.2:c.4131+162G=
|
NP_982284.1:n.4131+162G=
|
|
XM_005245041.2:c.4116+162G=
|
XP_005245098.1:n.4116+162G=
|
|
XM_005245041.3:c.4116+162G=
|
XP_005245098.1:n.4116+162G=
|
|
XM_017000799.1:c.3831+162G=
|
XP_016856288.1:n.3831+162G=
|
|
NM_001297707.2:c.4164+162G=
|
NP_001284636.1:n.4164+162G=
|
|
NM_001297708.2:c.4083+162G=
|
NP_001284637.1:n.4083+162G=
|
|
NM_203459.3:c.4131+162G=
|
NP_982284.1:n.4131+162G=
|
|
NM_001297707.3:c.4164+162G=
|
NP_001284636.1:n.4164+162G=
|
|
NM_001297708.3:c.4083+162G=
|
NP_001284637.1:n.4083+162G=
|
|
NM_001389638.1:c.4116+162G=
|
NP_001376567.1:n.4116+162G=
|
|
NM_203459.4:c.4131+162G=
MANE Select
|
NP_982284.1:n.4131+162G=
|
|