ENST00000374479.4:c.1128G>A
MANE Select
|
ENSP00000363603.3:p.Arg376=
|
|
ENST00000374479.3:c.1128G>A
|
ENSP00000363603.3:p.Arg376=
|
|
NM_000147.4:c.1128G>A
|
NP_000138.2:p.Arg376=
|
|
XM_005245821.1:c.753G>A
|
XP_005245878.1:p.Arg251=
|
|
XM_011541167.1:c.495G>A
|
XP_011539469.1:p.Arg165=
|
|
XM_005245821.3:c.753G>A
|
XP_005245878.1:p.Arg251=
|
|
XM_011541167.3:c.495G>A
|
XP_011539469.1:p.Arg165=
|
|
XM_017000905.2:c.825G>A
|
XP_016856394.1:p.Arg275=
|
|
NM_000147.5:c.1128G>A
MANE Select
|
NP_000138.2:p.Arg376=
|
|
NR_174379.1:n.1306G>A
|
|
|
NR_174380.1:n.1355G>A
|
|
|
NR_174381.1:n.1194G>A
|
|
|
NR_174382.1:n.1591G>A
|
|
|