ENST00000309383.6:c.2121G>A
MANE Select
|
ENSP00000310649.1:p.Glu707=
|
|
ENST00000309383.5:c.2121G>A
|
ENSP00000310649.1:p.Glu707=
|
|
ENST00000326848.7:c.1206G>A
|
ENSP00000320853.7:p.Glu402=
|
|
ENST00000590333.5:c.2169G>A
|
ENSP00000468190.1:p.Glu723=
|
|
NM_032430.1:c.2121G>A
|
NP_115806.1:p.Glu707=
|
|
XM_005259327.2:c.1851G>A
|
XP_005259384.1:p.Glu617=
|
|
XM_011527395.1:c.1878G>A
|
XP_011525697.1:p.Glu626=
|
|
XR_430213.2:n.2104G>A
|
|
|
XM_005259327.3:c.1851G>A
|
XP_005259384.1:p.Glu617=
|
|
XM_011527395.2:c.1593G>A
|
XP_011525697.2:p.Glu531=
|
|
XM_024451739.1:c.1896G>A
|
XP_024307507.1:p.Glu632=
|
|
XR_430213.4:n.2402G>A
|
|
|
NM_032430.2:c.2121G>A
MANE Select
|
NP_115806.1:p.Glu707=
|
|