ENST00000688602.1:c.286A>G
|
|
|
ENST00000689936.1:c.268A>G
|
|
|
ENST00000359596.8:c.11876A>G
MANE Select
|
ENSP00000352608.2:p.Gln3959Arg
|
|
ENST00000355481.8:c.11861A>G
|
ENSP00000347667.3:p.Gln3954Arg
|
|
ENST00000359596.7:c.11876A>G
|
ENSP00000352608.2:p.Gln3959Arg
|
|
ENST00000360985.7:c.11858A>G
|
ENSP00000354254.4:p.Gln3953Arg
|
|
ENST00000593322.1:c.485A>G
|
|
|
ENST00000594335.5:c.5245A>G
|
|
|
NM_000540.2:c.11876A>G , LRG_766t1:c.11876A>G
|
NP_000531.2:p.Gln3959Arg
|
|
NM_001042723.1:c.11861A>G
|
NP_001036188.1:p.Gln3954Arg
|
|
XM_006723317.1:c.11858A>G
|
XP_006723380.1:p.Gln3953Arg
|
|
XM_006723319.1:c.11843A>G
|
XP_006723382.1:p.Gln3948Arg
|
|
XM_011527204.1:c.11873A>G
|
XP_011525506.1:p.Gln3958Arg
|
|
XM_011527205.1:c.11876A>G
|
XP_011525507.1:p.Gln3959Arg
|
|
XM_006723317.2:c.11858A>G
|
XP_006723380.1:p.Gln3953Arg
|
|
XM_006723319.2:c.11843A>G
|
XP_006723382.1:p.Gln3948Arg
|
|
XM_011527205.2:c.11876A>G
|
XP_011525507.1:p.Gln3959Arg
|
|
NM_000540.3:c.11876A>G
MANE Select
|
NP_000531.2:p.Gln3959Arg
|
|
NM_001042723.2:c.11861A>G
|
NP_001036188.1:p.Gln3954Arg
|
|