ENST00000688602.1:c.340A>C
|
|
|
ENST00000689936.1:c.322A>C
|
|
|
ENST00000359596.8:c.11930A>C
MANE Select
|
ENSP00000352608.2:p.Gln3977Pro
|
|
ENST00000355481.8:c.11915A>C
|
ENSP00000347667.3:p.Gln3972Pro
|
|
ENST00000359596.7:c.11930A>C
|
ENSP00000352608.2:p.Gln3977Pro
|
|
ENST00000360985.7:c.11912A>C
|
ENSP00000354254.4:p.Gln3971Pro
|
|
ENST00000593322.1:c.539A>C
|
|
|
ENST00000594335.5:c.5299A>C
|
|
|
NM_000540.2:c.11930A>C , LRG_766t1:c.11930A>C
|
NP_000531.2:p.Gln3977Pro
|
|
NM_001042723.1:c.11915A>C
|
NP_001036188.1:p.Gln3972Pro
|
|
XM_006723317.1:c.11912A>C
|
XP_006723380.1:p.Gln3971Pro
|
|
XM_006723319.1:c.11897A>C
|
XP_006723382.1:p.Gln3966Pro
|
|
XM_011527204.1:c.11927A>C
|
XP_011525506.1:p.Gln3976Pro
|
|
XM_011527205.1:c.11930A>C
|
XP_011525507.1:p.Gln3977Pro
|
|
XM_006723317.2:c.11912A>C
|
XP_006723380.1:p.Gln3971Pro
|
|
XM_006723319.2:c.11897A>C
|
XP_006723382.1:p.Gln3966Pro
|
|
XM_011527205.2:c.11930A>C
|
XP_011525507.1:p.Gln3977Pro
|
|
NM_000540.3:c.11930A>C
MANE Select
|
NP_000531.2:p.Gln3977Pro
|
|
NM_001042723.2:c.11915A>C
|
NP_001036188.1:p.Gln3972Pro
|
|