ENST00000328300.11:c.3818G>A
MANE Select
|
ENSP00000331902.7:p.Gly1273Asp
|
|
ENST00000361603.7:c.3800G>A
|
ENSP00000354505.2:p.Gly1267Asp
|
|
ENST00000510690.2:n.312G>A
|
|
|
ENST00000328300.10:c.3818G>A
|
ENSP00000331902.6:p.Gly1273Asp
|
|
ENST00000361603.6:c.3800G>A
|
ENSP00000354505.2:p.Gly1267Asp
|
|
ENST00000489230.1:n.221G>A
|
|
|
ENST00000510690.1:n.312G>A
|
|
|
NM_000495.4:c.3800G>A
|
NP_000486.1:p.Gly1267Asp
|
|
NM_033380.2:c.3818G>A
|
NP_203699.1:p.Gly1273Asp
|
|
XM_005262070.2:c.3809G>A
|
XP_005262127.1:p.Gly1270Asp
|
|
XM_006724616.2:c.3818G>A
|
XP_006724679.1:p.Gly1273Asp
|
|
XM_011530849.1:c.3494G>A
|
XP_011529151.1:p.Gly1165Asp
|
|
XM_011530851.1:c.1391G>A
|
XP_011529153.1:p.Gly464Asp
|
|
XM_011530849.2:c.3833G>A
|
XP_011529151.2:p.Gly1278Asp
|
|
XM_017029259.2:c.3824G>A
|
XP_016884748.1:p.Gly1275Asp
|
|
XM_017029260.1:c.3815G>A
|
XP_016884749.1:p.Gly1272Asp
|
|
XM_017029261.1:c.3833G>A
|
XP_016884750.1:p.Gly1278Asp
|
|
XM_017029263.2:c.2153G>A
|
XP_016884752.1:p.Gly718Asp
|
|
NM_000495.5:c.3800G>A
|
NP_000486.1:p.Gly1267Asp
|
|
NM_033380.3:c.3818G>A
MANE Select
|
NP_203699.1:p.Gly1273Asp
|
|