ENST00000649046.1:c.2469G=
MANE Select
|
ENSP00000496870.1:p.Gln823=
|
|
ENST00000263816.7:c.2469G=
|
ENSP00000263816.3:p.Gln823=
|
|
ENST00000443831.1:c.2058G=
|
ENSP00000409813.1:p.Gln686=
|
|
NM_004525.2:c.2469G=
|
NP_004516.2:p.Gln823=
|
|
XM_011511183.1:c.2469G=
|
XP_011509485.1:p.Gln823=
|
|
XM_011511184.1:c.180G=
|
XP_011509486.1:p.Gln60=
|
|
XM_011511185.1:c.2469G=
|
XP_011509487.1:p.Gln823=
|
|
NM_004525.3:c.2469G=
MANE Select
|
NP_004516.2:p.Gln823=
|
|
XM_011511183.3:c.2469G=
|
XP_011509485.1:p.Gln823=
|
|
XM_011511184.2:c.180G=
|
XP_011509486.1:p.Gln60=
|
|