ENST00000688602.1:c.187A>G
|
|
|
ENST00000689936.1:c.169A>G
|
|
|
ENST00000359596.8:c.11777A>G
MANE Select
|
ENSP00000352608.2:p.Gln3926Arg
|
|
ENST00000355481.8:c.11762A>G
|
ENSP00000347667.3:p.Gln3921Arg
|
|
ENST00000359596.7:c.11777A>G
|
ENSP00000352608.2:p.Gln3926Arg
|
|
ENST00000360985.7:c.11759A>G
|
ENSP00000354254.4:p.Gln3920Arg
|
|
ENST00000593322.1:c.386A>G
|
|
|
ENST00000594335.5:c.5146A>G
|
|
|
NM_000540.2:c.11777A>G , LRG_766t1:c.11777A>G
|
NP_000531.2:p.Gln3926Arg
|
|
NM_001042723.1:c.11762A>G
|
NP_001036188.1:p.Gln3921Arg
|
|
XM_006723317.1:c.11759A>G
|
XP_006723380.1:p.Gln3920Arg
|
|
XM_006723319.1:c.11744A>G
|
XP_006723382.1:p.Gln3915Arg
|
|
XM_011527204.1:c.11774A>G
|
XP_011525506.1:p.Gln3925Arg
|
|
XM_011527205.1:c.11777A>G
|
XP_011525507.1:p.Gln3926Arg
|
|
XM_006723317.2:c.11759A>G
|
XP_006723380.1:p.Gln3920Arg
|
|
XM_006723319.2:c.11744A>G
|
XP_006723382.1:p.Gln3915Arg
|
|
XM_011527205.2:c.11777A>G
|
XP_011525507.1:p.Gln3926Arg
|
|
NM_000540.3:c.11777A>G
MANE Select
|
NP_000531.2:p.Gln3926Arg
|
|
NM_001042723.2:c.11762A>G
|
NP_001036188.1:p.Gln3921Arg
|
|