ENST00000309383.6:c.2119G>T
MANE Select
|
ENSP00000310649.1:p.Glu707Ter
|
|
ENST00000309383.5:c.2119G>T
|
ENSP00000310649.1:p.Glu707Ter
|
|
ENST00000326848.7:c.1204G>T
|
ENSP00000320853.7:p.Glu402Ter
|
|
ENST00000590333.5:c.2167G>T
|
ENSP00000468190.1:p.Glu723Ter
|
|
NM_032430.1:c.2119G>T
|
NP_115806.1:p.Glu707Ter
|
|
XM_005259327.2:c.1849G>T
|
XP_005259384.1:p.Glu617Ter
|
|
XM_011527395.1:c.1876G>T
|
XP_011525697.1:p.Glu626Ter
|
|
XR_430213.2:n.2102G>T
|
|
|
XM_005259327.3:c.1849G>T
|
XP_005259384.1:p.Glu617Ter
|
|
XM_011527395.2:c.1591G>T
|
XP_011525697.2:p.Glu531Ter
|
|
XM_024451739.1:c.1894G>T
|
XP_024307507.1:p.Glu632Ter
|
|
XR_430213.4:n.2400G>T
|
|
|
NM_032430.2:c.2119G>T
MANE Select
|
NP_115806.1:p.Glu707Ter
|
|