ENST00000593677.2:c.1002T>C
|
|
|
ENST00000688602.1:c.2399T>C
|
|
|
ENST00000689936.1:c.2371T>C
|
|
|
ENST00000359596.8:c.14066T>C
MANE Select
|
ENSP00000352608.2:p.Ile4689Thr
|
|
ENST00000355481.8:c.14051T>C
|
ENSP00000347667.3:p.Ile4684Thr
|
|
ENST00000359596.7:c.14066T>C
|
ENSP00000352608.2:p.Ile4689Thr
|
|
ENST00000360985.7:c.14048T>C
|
ENSP00000354254.4:p.Ile4683Thr
|
|
NM_000540.2:c.14066T>C , LRG_766t1:c.14066T>C
|
NP_000531.2:p.Ile4689Thr
|
|
NM_001042723.1:c.14051T>C
|
NP_001036188.1:p.Ile4684Thr
|
|
XM_006723317.1:c.14048T>C
|
XP_006723380.1:p.Ile4683Thr
|
|
XM_006723319.1:c.14033T>C
|
XP_006723382.1:p.Ile4678Thr
|
|
XM_011527204.1:c.14063T>C
|
XP_011525506.1:p.Ile4688Thr
|
|
XM_011527205.1:c.13979T>C
|
XP_011525507.1:p.Ile4660Thr
|
|
XM_006723317.2:c.14048T>C
|
XP_006723380.1:p.Ile4683Thr
|
|
XM_006723319.2:c.14033T>C
|
XP_006723382.1:p.Ile4678Thr
|
|
XM_011527205.2:c.13979T>C
|
XP_011525507.1:p.Ile4660Thr
|
|
NM_000540.3:c.14066T>C
MANE Select
|
NP_000531.2:p.Ile4689Thr
|
|
NM_001042723.2:c.14051T>C
|
NP_001036188.1:p.Ile4684Thr
|
|