ENST00000374479.4:c.1092C=
MANE Select
|
ENSP00000363603.3:p.Ile364=
|
|
ENST00000374479.3:c.1092C=
|
ENSP00000363603.3:p.Ile364=
|
|
NM_000147.4:c.1092C=
|
NP_000138.2:p.Ile364=
|
|
XM_005245821.1:c.717C=
|
XP_005245878.1:p.Ile239=
|
|
XM_011541167.1:c.459C=
|
XP_011539469.1:p.Ile153=
|
|
XM_005245821.3:c.717C=
|
XP_005245878.1:p.Ile239=
|
|
XM_011541167.3:c.459C=
|
XP_011539469.1:p.Ile153=
|
|
XM_017000905.2:c.789C=
|
XP_016856394.1:p.Ile263=
|
|
NM_000147.5:c.1092C=
MANE Select
|
NP_000138.2:p.Ile364=
|
|
NR_174379.1:n.1270C=
|
|
|
NR_174380.1:n.1319C=
|
|
|
NR_174381.1:n.1158C=
|
|
|
NR_174382.1:n.1555C=
|
|
|