ENST00000649046.1:c.12228G=
MANE Select
|
ENSP00000496870.1:p.Glu4076=
|
|
ENST00000649153.1:c.3128G=
|
|
|
ENST00000650252.1:c.1256G=
|
ENSP00000496887.1:p.Ser419=
|
|
ENST00000263816.7:c.12228G=
|
ENSP00000263816.3:p.Glu4076=
|
|
NM_004525.2:c.12228G=
|
NP_004516.2:p.Glu4076=
|
|
XM_011511183.1:c.12099G=
|
XP_011509485.1:p.Glu4033=
|
|
XM_011511184.1:c.9939G=
|
XP_011509486.1:p.Glu3313=
|
|
NM_004525.3:c.12228G=
MANE Select
|
NP_004516.2:p.Glu4076=
|
|
XM_011511183.3:c.12099G=
|
XP_011509485.1:p.Glu4033=
|
|
XM_011511184.2:c.9939G=
|
XP_011509486.1:p.Glu3313=
|
|