ENST00000374479.4:c.1130T>A
MANE Select
|
ENSP00000363603.3:p.Val377Glu
|
|
ENST00000374479.3:c.1130T>A
|
ENSP00000363603.3:p.Val377Glu
|
|
NM_000147.4:c.1130T>A
|
NP_000138.2:p.Val377Glu
|
|
XM_005245821.1:c.755T>A
|
XP_005245878.1:p.Val252Glu
|
|
XM_011541167.1:c.497T>A
|
XP_011539469.1:p.Val166Glu
|
|
XM_005245821.3:c.755T>A
|
XP_005245878.1:p.Val252Glu
|
|
XM_011541167.3:c.497T>A
|
XP_011539469.1:p.Val166Glu
|
|
XM_017000905.2:c.827T>A
|
XP_016856394.1:p.Val276Glu
|
|
NM_000147.5:c.1130T>A
MANE Select
|
NP_000138.2:p.Val377Glu
|
|
NR_174379.1:n.1308T>A
|
|
|
NR_174380.1:n.1357T>A
|
|
|
NR_174381.1:n.1196T>A
|
|
|
NR_174382.1:n.1593T>A
|
|
|