ENST00000374479.4:c.1096G=
MANE Select
|
ENSP00000363603.3:p.Gly366=
|
|
ENST00000374479.3:c.1096G=
|
ENSP00000363603.3:p.Gly366=
|
|
NM_000147.4:c.1096G=
|
NP_000138.2:p.Gly366=
|
|
XM_005245821.1:c.721G=
|
XP_005245878.1:p.Gly241=
|
|
XM_011541167.1:c.463G=
|
XP_011539469.1:p.Gly155=
|
|
XM_005245821.3:c.721G=
|
XP_005245878.1:p.Gly241=
|
|
XM_011541167.3:c.463G=
|
XP_011539469.1:p.Gly155=
|
|
XM_017000905.2:c.793G=
|
XP_016856394.1:p.Gly265=
|
|
NM_000147.5:c.1096G=
MANE Select
|
NP_000138.2:p.Gly366=
|
|
NR_174379.1:n.1274G=
|
|
|
NR_174380.1:n.1323G=
|
|
|
NR_174381.1:n.1162G=
|
|
|
NR_174382.1:n.1559G=
|
|
|