ENST00000374479.4:c.1098G>C
MANE Select
|
ENSP00000363603.3:p.Gly366=
|
|
ENST00000374479.3:c.1098G>C
|
ENSP00000363603.3:p.Gly366=
|
|
NM_000147.4:c.1098G>C
|
NP_000138.2:p.Gly366=
|
|
XM_005245821.1:c.723G>C
|
XP_005245878.1:p.Gly241=
|
|
XM_011541167.1:c.465G>C
|
XP_011539469.1:p.Gly155=
|
|
XM_005245821.3:c.723G>C
|
XP_005245878.1:p.Gly241=
|
|
XM_011541167.3:c.465G>C
|
XP_011539469.1:p.Gly155=
|
|
XM_017000905.2:c.795G>C
|
XP_016856394.1:p.Gly265=
|
|
NM_000147.5:c.1098G>C
MANE Select
|
NP_000138.2:p.Gly366=
|
|
NR_174379.1:n.1276G>C
|
|
|
NR_174380.1:n.1325G>C
|
|
|
NR_174381.1:n.1164G>C
|
|
|
NR_174382.1:n.1561G>C
|
|
|