ENST00000359271.4:c.174T>G
MANE Select
|
ENSP00000352216.2:p.Ala58=
|
|
ENST00000359271.3:c.174T>G
|
ENSP00000352216.2:p.Ala58=
|
|
ENST00000611837.1:n.326T>G
|
|
|
NM_030777.3:c.174T>G
|
NP_110404.1:p.Ala58=
|
|
XM_011529060.1:c.237T>G
|
XP_011527362.1:p.Ala79=
|
|
XM_011529061.1:c.183T>G
|
XP_011527363.1:p.Ala61=
|
|
XM_011529062.1:c.237T>G
|
XP_011527364.1:p.Ala79=
|
|
XM_011529063.1:c.237T>G
|
XP_011527365.1:p.Ala79=
|
|
XM_011529064.1:c.237T>G
|
XP_011527366.1:p.Ala79=
|
|
XM_011529065.1:c.237T>G
|
XP_011527367.1:p.Ala79=
|
|
XR_936641.1:n.373T>G
|
|
|
XM_011529060.2:c.237T>G
|
XP_011527362.1:p.Ala79=
|
|
XM_011529061.2:c.183T>G
|
XP_011527363.1:p.Ala61=
|
|
XM_011529062.2:c.237T>G
|
XP_011527364.1:p.Ala79=
|
|
XM_011529063.2:c.237T>G
|
XP_011527365.1:p.Ala79=
|
|
XM_011529064.2:c.237T>G
|
XP_011527366.1:p.Ala79=
|
|
XM_011529065.2:c.237T>G
|
XP_011527367.1:p.Ala79=
|
|
XM_017028087.2:c.174T>G
|
XP_016883576.1:p.Ala58=
|
|
XR_936641.2:n.360T>G
|
|
|
NM_030777.4:c.174T>G
MANE Select
|
NP_110404.1:p.Ala58=
|
|