ENST00000338639.10:c.468G>T
MANE Select
|
ENSP00000340278.5:p.Arg156=
|
|
ENST00000338639.9:c.468G>T
|
ENSP00000340278.5:p.Arg156=
|
|
ENST00000377488.5:c.468G>T
|
ENSP00000366708.1:p.Arg156=
|
|
ENST00000377491.5:c.468G>T
|
ENSP00000366711.1:p.Arg156=
|
|
ENST00000377493.9:c.408G>T
|
ENSP00000466242.1:p.Arg136=
|
|
ENST00000469225.1:c.381G>T
|
ENSP00000466756.1:p.Arg127=
|
|
ENST00000493373.5:c.468G>T
|
ENSP00000465404.1:p.Arg156=
|
|
ENST00000493678.5:c.468G>T
|
ENSP00000418770.1:p.Arg156=
|
|
NM_001123377.1:c.468G>T
|
NP_001116849.1:p.Arg156=
|
|
NM_007262.4:c.468G>T
|
NP_009193.2:p.Arg156=
|
|
XM_005263424.2:c.468G>T
|
XP_005263481.1:p.Arg156=
|
|
XM_005263424.3:c.468G>T
|
XP_005263481.1:p.Arg156=
|
|
NM_007262.5:c.468G>T
MANE Select
|
NP_009193.2:p.Arg156=
|
|
NM_001123377.2:c.468G>T
|
NP_001116849.1:p.Arg156=
|
|