ENST00000359271.4:c.1340C=
MANE Select
|
ENSP00000352216.2:p.Ala447=
|
|
ENST00000359271.3:c.1340C=
|
ENSP00000352216.2:p.Ala447=
|
|
NM_030777.3:c.1340C=
|
NP_110404.1:p.Ala447=
|
|
XM_011529060.1:c.1403C=
|
XP_011527362.1:p.Ala468=
|
|
XM_011529061.1:c.1349C=
|
XP_011527363.1:p.Ala450=
|
|
XM_011529062.1:c.1452C=
|
XP_011527364.1:p.Ser484=
|
|
XM_011529063.1:c.1403C=
|
XP_011527365.1:p.Ala468=
|
|
XM_011529064.1:c.1452C=
|
XP_011527366.1:p.Ser484=
|
|
XM_011529065.1:c.1403C=
|
XP_011527367.1:p.Ala468=
|
|
XR_936641.1:n.1588C=
|
|
|
XM_011529060.2:c.1403C=
|
XP_011527362.1:p.Ala468=
|
|
XM_011529061.2:c.1349C=
|
XP_011527363.1:p.Ala450=
|
|
XM_011529062.2:c.1452C=
|
XP_011527364.1:p.Ser484=
|
|
XM_011529063.2:c.1403C=
|
XP_011527365.1:p.Ala468=
|
|
XM_011529064.2:c.1452C=
|
XP_011527366.1:p.Ser484=
|
|
XM_011529065.2:c.1403C=
|
XP_011527367.1:p.Ala468=
|
|
XM_017028087.2:c.1340C=
|
XP_016883576.1:p.Ala447=
|
|
XR_936641.2:n.1575C=
|
|
|
NM_030777.4:c.1340C=
MANE Select
|
NP_110404.1:p.Ala447=
|
|