ENST00000360228.11:c.5016T>G
MANE Select
|
ENSP00000353362.5:p.Arg1672=
|
|
ENST00000573710.7:c.5022T>G
|
ENSP00000460092.3:p.Arg1674=
|
|
ENST00000573891.6:c.435T>G
|
|
|
ENST00000574822.6:n.240T>G
|
|
|
ENST00000585802.6:c.177T>G
|
ENSP00000465598.2:p.Arg59=
|
|
ENST00000593267.2:n.221T>G
|
|
|
ENST00000635727.1:c.5019T>G
|
ENSP00000490001.1:p.Arg1673=
|
|
ENST00000635742.1:n.1005T>G
|
|
|
ENST00000635895.1:c.5019T>G
|
ENSP00000490323.1:p.Arg1673=
|
|
ENST00000636012.1:c.5019T>G
|
ENSP00000490223.1:p.Arg1673=
|
|
ENST00000636058.1:c.331T>G
|
|
|
ENST00000636389.1:c.5019T>G
|
ENSP00000489992.1:p.Arg1673=
|
|
ENST00000636473.1:c.177T>G
|
ENSP00000490173.1:p.Arg59=
|
|
ENST00000636549.1:c.5025T>G
|
ENSP00000490578.1:p.Arg1675=
|
|
ENST00000637276.1:c.5019T>G
|
ENSP00000489777.1:p.Arg1673=
|
|
ENST00000637297.1:c.312T>G
|
ENSP00000489692.1:p.Arg104=
|
|
ENST00000637432.1:c.5034T>G
|
ENSP00000490617.1:p.Arg1678=
|
|
ENST00000637736.1:c.4878T>G
|
ENSP00000489861.1:p.Arg1626=
|
|
ENST00000637769.1:c.5019T>G
|
ENSP00000489778.1:p.Arg1673=
|
|
ENST00000637777.1:c.276T>G
|
|
|
ENST00000637809.1:n.409T>G
|
|
|
ENST00000637819.1:c.420T>G
|
ENSP00000490686.1:p.Arg140=
|
|
ENST00000637832.1:n.10T>G
|
|
|
ENST00000637927.1:c.5022T>G
|
ENSP00000489715.1:p.Arg1674=
|
|
ENST00000638009.2:c.5019T>G
|
ENSP00000489913.1:p.Arg1673=
|
|
ENST00000638029.1:c.5034T>G
|
ENSP00000489829.1:p.Arg1678=
|
|
ENST00000664864.1:c.5220T>G
|
ENSP00000499449.1:p.Arg1740=
|
|
ENST00000360228.9:c.5016T>G
|
ENSP00000353362.5:p.Arg1672=
|
|
ENST00000573710.6:c.5019T>G
|
ENSP00000460092.2:p.Arg1673=
|
|
ENST00000573891.5:c.435T>G
|
|
|
ENST00000574822.5:n.240T>G
|
|
|
ENST00000585802.5:c.1074T>G
|
ENSP00000465598.1:p.Arg358=
|
|
ENST00000587525.5:c.477T>G
|
ENSP00000467729.1:p.Arg159=
|
|
ENST00000593267.1:n.221T>G
|
|
|
ENST00000614285.4:c.5034T>G
|
ENSP00000479983.1:p.Arg1678=
|
|
NM_000068.3:c.5034T>G
|
NP_000059.3:p.Arg1678=
|
|
NM_001127221.1:c.5019T>G , LRG_7t1:c.5019T>G
|
NP_001120693.1:p.Arg1673=
|
|
NM_001127222.1:c.5016T>G
|
NP_001120694.1:p.Arg1672=
|
|
NM_001174080.1:c.5025T>G
|
NP_001167551.1:p.Arg1675=
|
|
NM_023035.2:c.5034T>G
|
NP_075461.2:p.Arg1678=
|
|
NM_000068.4:c.5034T>G
|
NP_000059.3:p.Arg1678=
|
|
NM_001127222.2:c.5016T>G
MANE Select
|
NP_001120694.1:p.Arg1672=
|
|
NM_001174080.2:c.5025T>G
|
NP_001167551.1:p.Arg1675=
|
|
NM_023035.3:c.5034T>G
|
NP_075461.2:p.Arg1678=
|
|
NM_001127221.2:c.5019T>G
|
NP_001120693.1:p.Arg1673=
|
|