ENST00000355699.7:c.3058T>A
MANE Select
|
ENSP00000347927.2:p.Ser1020Thr
|
|
ENST00000355699.6:c.3058T>A
|
ENSP00000347927.2:p.Ser1020Thr
|
|
ENST00000356589.6:c.2965T>A
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ENSP00000348997.2:p.Ser989Thr
|
|
ENST00000371916.5:c.*527T>A
|
ENSP00000360984.2:n.*527T>A
|
|
ENST00000371929.7:c.3058T>A
|
ENSP00000360997.3:p.Ser1020Thr
|
|
ENST00000485925.5:n.1874T>A
|
|
|
NM_139025.4:c.3058T>A , LRG_544t1:c.3058T>A
|
NP_620594.1:p.Ser1020Thr
|
|
NM_139026.4:c.2965T>A
|
NP_620595.1:p.Ser989Thr
|
|
NM_139027.4:c.3058T>A
|
NP_620596.2:p.Ser1020Thr
|
|
NR_024514.2:n.1893T>A
|
|
|
XM_011518174.1:c.2668T>A
|
XP_011516476.1:p.Ser890Thr
|
|
XM_011518175.1:c.3058T>A
|
XP_011516477.1:p.Ser1020Thr
|
|
XM_011518176.1:c.2074T>A
|
XP_011516478.1:p.Ser692Thr
|
|
XM_011518177.1:c.2068T>A
|
XP_011516479.1:p.Ser690Thr
|
|
XM_011518178.1:c.1723T>A
|
XP_011516480.1:p.Ser575Thr
|
|
XM_011518179.1:c.1723T>A
|
XP_011516481.1:p.Ser575Thr
|
|
XM_011518180.1:c.1324T>A
|
XP_011516482.1:p.Ser442Thr
|
|
XM_011518176.3:c.2074T>A
|
XP_011516478.1:p.Ser692Thr
|
|
XM_011518178.2:c.1723T>A
|
XP_011516480.1:p.Ser575Thr
|
|
XM_017014232.1:c.3046T>A
|
XP_016869721.1:p.Ser1016Thr
|
|
XM_017014233.1:c.2668T>A
|
XP_016869722.1:p.Ser890Thr
|
|
XM_017014234.2:c.2068T>A
|
XP_016869723.1:p.Ser690Thr
|
|
XR_001746171.1:n.3831T>A
|
|
|
NM_139026.5:c.2965T>A
|
NP_620595.1:p.Ser989Thr
|
|
NM_139027.5:c.3058T>A
|
NP_620596.2:p.Ser1020Thr
|
|
NM_139025.5:c.3058T>A
|
NP_620594.1:p.Ser1020Thr
|
|
NM_139026.6:c.2965T>A
|
NP_620595.1:p.Ser989Thr
|
|
NM_139027.6:c.3058T>A
MANE Select
|
NP_620596.2:p.Ser1020Thr
|
|
NR_024514.3:n.1895T>A
|
|
|