ENST00000593677.2:c.908T=
|
|
|
ENST00000688602.1:c.2305T=
|
|
|
ENST00000689936.1:c.2277T=
|
|
|
ENST00000359596.8:c.13972T=
MANE Select
|
ENSP00000352608.2:p.Cys4658=
|
|
ENST00000355481.8:c.13957T=
|
ENSP00000347667.3:p.Cys4653=
|
|
ENST00000359596.7:c.13972T=
|
ENSP00000352608.2:p.Cys4658=
|
|
ENST00000360985.7:c.13954T=
|
ENSP00000354254.4:p.Cys4652=
|
|
ENST00000593677.1:c.432T=
|
|
|
NM_000540.2:c.13972T= , LRG_766t1:c.13972T=
|
NP_000531.2:p.Cys4658=
|
|
NM_001042723.1:c.13957T=
|
NP_001036188.1:p.Cys4653=
|
|
XM_006723317.1:c.13954T=
|
XP_006723380.1:p.Cys4652=
|
|
XM_006723319.1:c.13939T=
|
XP_006723382.1:p.Cys4647=
|
|
XM_011527204.1:c.13969T=
|
XP_011525506.1:p.Cys4657=
|
|
XM_011527205.1:c.13885T=
|
XP_011525507.1:p.Cys4629=
|
|
XM_006723317.2:c.13954T=
|
XP_006723380.1:p.Cys4652=
|
|
XM_006723319.2:c.13939T=
|
XP_006723382.1:p.Cys4647=
|
|
XM_011527205.2:c.13885T=
|
XP_011525507.1:p.Cys4629=
|
|
NM_000540.3:c.13972T=
MANE Select
|
NP_000531.2:p.Cys4658=
|
|
NM_001042723.2:c.13957T=
|
NP_001036188.1:p.Cys4653=
|
|