ENST00000309383.6:c.2171C>A
MANE Select
|
ENSP00000310649.1:p.Ala724Asp
|
|
ENST00000309383.5:c.2171C>A
|
ENSP00000310649.1:p.Ala724Asp
|
|
ENST00000326848.7:c.1256C>A
|
ENSP00000320853.7:p.Ala419Asp
|
|
ENST00000590333.5:c.2219C>A
|
ENSP00000468190.1:p.Ala740Asp
|
|
NM_032430.1:c.2171C>A
|
NP_115806.1:p.Ala724Asp
|
|
XM_005259327.2:c.1901C>A
|
XP_005259384.1:p.Ala634Asp
|
|
XM_011527395.1:c.1928C>A
|
XP_011525697.1:p.Ala643Asp
|
|
XR_430213.2:n.2154C>A
|
|
|
XM_005259327.3:c.1901C>A
|
XP_005259384.1:p.Ala634Asp
|
|
XM_011527395.2:c.1643C>A
|
XP_011525697.2:p.Ala548Asp
|
|
XM_024451739.1:c.1946C>A
|
XP_024307507.1:p.Ala649Asp
|
|
XR_430213.4:n.2452C>A
|
|
|
NM_032430.2:c.2171C>A
MANE Select
|
NP_115806.1:p.Ala724Asp
|
|