ENST00000377122.9:c.127A>G
MANE Select
|
ENSP00000366326.4:p.Arg43Gly
|
|
ENST00000674540.1:n.414A>G
|
|
|
ENST00000675114.1:n.565+64688A>G
|
|
|
ENST00000675700.1:n.380+64688A>G
|
|
|
ENST00000675702.1:n.636+64688A>G
|
|
|
ENST00000675747.1:n.2489A>G
|
|
|
ENST00000377119.5:n.137A>G
|
|
|
ENST00000377122.8:c.127A>G
|
ENSP00000366326.4:p.Arg43Gly
|
|
ENST00000417816.2:c.357+64688A>G
|
ENSP00000393896.2:n.357+64688A>G
|
|
ENST00000434381.1:c.79A>G
|
ENSP00000396512.1:p.Arg27Gly
|
|
NM_001173484.1:c.357+64688A>G
|
NP_001166955.1:n.357+64688A>G
|
|
NM_006393.2:c.127A>G , LRG_411t2:c.127A>G
|
NP_006384.1:p.Arg43Gly
|
|
NM_213569.2:c.357+64688A>G , LRG_411t1:c.357+64688A>G
|
NP_998734.1:n.357+64688A>G
|
|
XM_005252342.3:c.127A>G
|
XP_005252399.1:p.Arg43Gly
|
|
XM_005252343.3:c.127A>G
|
XP_005252400.1:p.Arg43Gly
|
|
XM_005252344.3:c.127A>G
|
XP_005252401.1:p.Arg43Gly
|
|
XM_011519290.1:c.79A>G
|
XP_011517592.1:p.Arg27Gly
|
|
XM_011519291.1:c.79A>G
|
XP_011517593.1:p.Arg27Gly
|
|
XR_242691.3:n.239A>G
|
|
|
XM_005252342.5:c.127A>G
|
XP_005252399.1:p.Arg43Gly
|
|
XM_005252343.5:c.127A>G
|
XP_005252400.1:p.Arg43Gly
|
|
XM_005252344.5:c.127A>G
|
XP_005252401.1:p.Arg43Gly
|
|
XM_011519291.2:c.79A>G
|
XP_011517593.1:p.Arg27Gly
|
|
XM_017015468.1:c.79A>G
|
XP_016870957.1:p.Arg27Gly
|
|
XR_001746995.2:n.1723A>G
|
|
|
XR_001746996.1:n.442A>G
|
|
|
XR_242691.5:n.1723A>G
|
|
|
NM_001173484.2:c.357+64688A>G
|
NP_001166955.1:n.357+64688A>G
|
|
NM_001377322.1:c.357+64688A>G
|
NP_001364251.1:n.357+64688A>G
|
|
NM_001377323.1:c.309+64688A>G
|
NP_001364252.1:n.309+64688A>G
|
|
NM_001377324.1:c.300+64688A>G
|
NP_001364253.1:n.300+64688A>G
|
|
NM_001377325.1:c.291+64688A>G
|
NP_001364254.1:n.291+64688A>G
|
|
NM_001377326.1:c.249+64688A>G
|
NP_001364255.1:n.249+64688A>G
|
|
NM_001377327.1:c.249+64688A>G
|
NP_001364256.1:n.249+64688A>G
|
|
NM_001377328.1:c.249+64688A>G
|
NP_001364257.1:n.249+64688A>G
|
|
NM_006393.3:c.127A>G
MANE Select
|
NP_006384.1:p.Arg43Gly
|
|