ENST00000593677.2:c.1179C>G
|
|
|
ENST00000688602.1:c.2576C>G
|
|
|
ENST00000689936.1:c.2548C>G
|
|
|
ENST00000359596.8:c.14243C>G
MANE Select
|
ENSP00000352608.2:p.Thr4748Arg
|
|
ENST00000355481.8:c.14228C>G
|
ENSP00000347667.3:p.Thr4743Arg
|
|
ENST00000359596.7:c.14243C>G
|
ENSP00000352608.2:p.Thr4748Arg
|
|
ENST00000360985.7:c.14225C>G
|
ENSP00000354254.4:p.Thr4742Arg
|
|
NM_000540.2:c.14243C>G , LRG_766t1:c.14243C>G
|
NP_000531.2:p.Thr4748Arg
|
|
NM_001042723.1:c.14228C>G
|
NP_001036188.1:p.Thr4743Arg
|
|
XM_006723317.1:c.14225C>G
|
XP_006723380.1:p.Thr4742Arg
|
|
XM_006723319.1:c.14210C>G
|
XP_006723382.1:p.Thr4737Arg
|
|
XM_011527204.1:c.14240C>G
|
XP_011525506.1:p.Thr4747Arg
|
|
XM_011527205.1:c.14156C>G
|
XP_011525507.1:p.Thr4719Arg
|
|
XM_006723317.2:c.14225C>G
|
XP_006723380.1:p.Thr4742Arg
|
|
XM_006723319.2:c.14210C>G
|
XP_006723382.1:p.Thr4737Arg
|
|
XM_011527205.2:c.14156C>G
|
XP_011525507.1:p.Thr4719Arg
|
|
NM_000540.3:c.14243C>G
MANE Select
|
NP_000531.2:p.Thr4748Arg
|
|
NM_001042723.2:c.14228C>G
|
NP_001036188.1:p.Thr4743Arg
|
|