ENST00000309383.6:c.2120A>T
MANE Select
|
ENSP00000310649.1:p.Glu707Val
|
|
ENST00000309383.5:c.2120A>T
|
ENSP00000310649.1:p.Glu707Val
|
|
ENST00000326848.7:c.1205A>T
|
ENSP00000320853.7:p.Glu402Val
|
|
ENST00000590333.5:c.2168A>T
|
ENSP00000468190.1:p.Glu723Val
|
|
NM_032430.1:c.2120A>T
|
NP_115806.1:p.Glu707Val
|
|
XM_005259327.2:c.1850A>T
|
XP_005259384.1:p.Glu617Val
|
|
XM_011527395.1:c.1877A>T
|
XP_011525697.1:p.Glu626Val
|
|
XR_430213.2:n.2103A>T
|
|
|
XM_005259327.3:c.1850A>T
|
XP_005259384.1:p.Glu617Val
|
|
XM_011527395.2:c.1592A>T
|
XP_011525697.2:p.Glu531Val
|
|
XM_024451739.1:c.1895A>T
|
XP_024307507.1:p.Glu632Val
|
|
XR_430213.4:n.2401A>T
|
|
|
NM_032430.2:c.2120A>T
MANE Select
|
NP_115806.1:p.Glu707Val
|
|