ENST00000374479.4:c.1131G>C
MANE Select
|
ENSP00000363603.3:p.Val377=
|
|
ENST00000374479.3:c.1131G>C
|
ENSP00000363603.3:p.Val377=
|
|
NM_000147.4:c.1131G>C
|
NP_000138.2:p.Val377=
|
|
XM_005245821.1:c.756G>C
|
XP_005245878.1:p.Val252=
|
|
XM_011541167.1:c.498G>C
|
XP_011539469.1:p.Val166=
|
|
XM_005245821.3:c.756G>C
|
XP_005245878.1:p.Val252=
|
|
XM_011541167.3:c.498G>C
|
XP_011539469.1:p.Val166=
|
|
XM_017000905.2:c.828G>C
|
XP_016856394.1:p.Val276=
|
|
NM_000147.5:c.1131G>C
MANE Select
|
NP_000138.2:p.Val377=
|
|
NR_174379.1:n.1309G>C
|
|
|
NR_174380.1:n.1358G>C
|
|
|
NR_174381.1:n.1197G>C
|
|
|
NR_174382.1:n.1594G>C
|
|
|