ENST00000324041.6:c.566G=
MANE Select
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ENSP00000326159.1:p.Ser189=
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ENST00000324041.5:c.566G=
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ENSP00000326159.1:p.Ser189=
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ENST00000431178.2:c.328+174G=
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ENSP00000399448.2:n.328+174G=
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ENST00000593885.1:c.*61G=
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ENSP00000469769.1:n.*61G=
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ENST00000596876.1:n.568G=
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ENST00000598305.5:c.*61G=
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ENSP00000469963.1:n.*61G=
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ENST00000599865.5:n.502G=
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ENST00000602148.1:c.578G=
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ENSP00000472091.1:n.578G=
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NM_001302961.1:c.281G=
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NP_001289890.1:p.Ser94=
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NM_004917.4:c.566G=
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NP_004908.4:p.Ser189=
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NR_126566.1:n.555G=
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XM_005259441.3:c.281G=
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XP_005259498.2:p.Ser94=
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XM_011527545.1:c.*61G=
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XP_011525847.1:n.*61G=
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XM_011527546.1:c.475+174G=
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XP_011525848.1:n.475+174G=
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XM_011527547.1:c.419G=
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XP_011525849.1:p.Ser140=
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XM_005259441.4:c.281G=
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XP_005259498.2:p.Ser94=
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XM_011527545.3:c.*61G=
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XP_011525847.1:n.*61G=
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|
XM_011527546.2:c.475+174G=
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XP_011525848.1:n.475+174G=
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|
NM_001302961.2:c.281G=
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NP_001289890.1:p.Ser94=
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|
NR_126566.2:n.555G=
|
|
|
NM_004917.5:c.566G=
MANE Select
|
NP_004908.4:p.Ser189=
|
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