ENST00000593677.2:c.1583T=
|
|
|
ENST00000688602.1:c.2980T=
|
|
|
ENST00000689936.1:c.2952T=
|
|
|
ENST00000692547.1:n.40T=
|
|
|
ENST00000359596.8:c.14647T=
MANE Select
|
ENSP00000352608.2:p.Cys4883=
|
|
ENST00000355481.8:c.14632T=
|
ENSP00000347667.3:p.Cys4878=
|
|
ENST00000359596.7:c.14647T=
|
ENSP00000352608.2:p.Cys4883=
|
|
ENST00000360985.7:c.14629T=
|
ENSP00000354254.4:p.Cys4877=
|
|
NM_000540.2:c.14647T= , LRG_766t1:c.14647T=
|
NP_000531.2:p.Cys4883=
|
|
NM_001042723.1:c.14632T=
|
NP_001036188.1:p.Cys4878=
|
|
XM_006723317.1:c.14629T=
|
XP_006723380.1:p.Cys4877=
|
|
XM_006723319.1:c.14614T=
|
XP_006723382.1:p.Cys4872=
|
|
XM_011527204.1:c.14644T=
|
XP_011525506.1:p.Cys4882=
|
|
XM_011527205.1:c.14560T=
|
XP_011525507.1:p.Cys4854=
|
|
XM_006723317.2:c.14629T=
|
XP_006723380.1:p.Cys4877=
|
|
XM_006723319.2:c.14614T=
|
XP_006723382.1:p.Cys4872=
|
|
XM_011527205.2:c.14560T=
|
XP_011525507.1:p.Cys4854=
|
|
NM_000540.3:c.14647T=
MANE Select
|
NP_000531.2:p.Cys4883=
|
|
NM_001042723.2:c.14632T=
|
NP_001036188.1:p.Cys4878=
|
|