ENST00000355699.7:c.3975A=
MANE Select
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ENSP00000347927.2:p.Ser1325=
|
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ENST00000355699.6:c.3975A=
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ENSP00000347927.2:p.Ser1325=
|
|
ENST00000356589.6:c.3882A=
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ENSP00000348997.2:p.Ser1294=
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ENST00000371910.1:c.531A=
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ENSP00000360978.1:p.Ser177=
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ENST00000371916.5:c.*1444A=
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ENSP00000360984.2:n.*1444A=
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ENST00000371929.7:c.4143A=
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ENSP00000360997.3:p.Ser1381=
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ENST00000485925.5:n.2606A=
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|
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NM_139025.4:c.4143A= , LRG_544t1:c.4143A=
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NP_620594.1:p.Ser1381=
|
|
NM_139026.4:c.3882A=
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NP_620595.1:p.Ser1294=
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|
NM_139027.4:c.3975A=
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NP_620596.2:p.Ser1325=
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|
NR_024514.2:n.2625A=
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|
|
XM_011518174.1:c.3753A=
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XP_011516476.1:p.Ser1251=
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|
XM_011518176.1:c.3159A=
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XP_011516478.1:p.Ser1053=
|
|
XM_011518177.1:c.3153A=
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XP_011516479.1:p.Ser1051=
|
|
XM_011518178.1:c.2808A=
|
XP_011516480.1:p.Ser936=
|
|
XM_011518179.1:c.2808A=
|
XP_011516481.1:p.Ser936=
|
|
XM_011518180.1:c.2409A=
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XP_011516482.1:p.Ser803=
|
|
XM_011518176.3:c.3159A=
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XP_011516478.1:p.Ser1053=
|
|
XM_011518178.2:c.2808A=
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XP_011516480.1:p.Ser936=
|
|
XM_017014232.1:c.4131A=
|
XP_016869721.1:p.Ser1377=
|
|
XM_017014233.1:c.3753A=
|
XP_016869722.1:p.Ser1251=
|
|
XM_017014234.2:c.3153A=
|
XP_016869723.1:p.Ser1051=
|
|
NM_139026.5:c.3882A=
|
NP_620595.1:p.Ser1294=
|
|
NM_139027.5:c.3975A=
|
NP_620596.2:p.Ser1325=
|
|
NM_139025.5:c.4143A=
|
NP_620594.1:p.Ser1381=
|
|
NM_139026.6:c.3882A=
|
NP_620595.1:p.Ser1294=
|
|
NM_139027.6:c.3975A=
MANE Select
|
NP_620596.2:p.Ser1325=
|
|
NR_024514.3:n.2627A=
|
|
|