ENST00000359271.4:c.466G>T
MANE Select
|
ENSP00000352216.2:p.Ala156Ser
|
|
ENST00000359271.3:c.466G>T
|
ENSP00000352216.2:p.Ala156Ser
|
|
NM_030777.3:c.466G>T
|
NP_110404.1:p.Ala156Ser
|
|
XM_011529060.1:c.529G>T
|
XP_011527362.1:p.Ala177Ser
|
|
XM_011529061.1:c.475G>T
|
XP_011527363.1:p.Ala159Ser
|
|
XM_011529062.1:c.529G>T
|
XP_011527364.1:p.Ala177Ser
|
|
XM_011529063.1:c.529G>T
|
XP_011527365.1:p.Ala177Ser
|
|
XM_011529064.1:c.529G>T
|
XP_011527366.1:p.Ala177Ser
|
|
XM_011529065.1:c.529G>T
|
XP_011527367.1:p.Ala177Ser
|
|
XR_936641.1:n.665G>T
|
|
|
XM_011529060.2:c.529G>T
|
XP_011527362.1:p.Ala177Ser
|
|
XM_011529061.2:c.475G>T
|
XP_011527363.1:p.Ala159Ser
|
|
XM_011529062.2:c.529G>T
|
XP_011527364.1:p.Ala177Ser
|
|
XM_011529063.2:c.529G>T
|
XP_011527365.1:p.Ala177Ser
|
|
XM_011529064.2:c.529G>T
|
XP_011527366.1:p.Ala177Ser
|
|
XM_011529065.2:c.529G>T
|
XP_011527367.1:p.Ala177Ser
|
|
XM_017028087.2:c.466G>T
|
XP_016883576.1:p.Ala156Ser
|
|
XR_936641.2:n.652G>T
|
|
|
NM_030777.4:c.466G>T
MANE Select
|
NP_110404.1:p.Ala156Ser
|
|