ENST00000358691.10:c.3278A>G
MANE Select
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ENSP00000351524.5:p.Glu1093Gly
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ENST00000358691.9:c.3278A>G
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ENSP00000351524.5:p.Glu1093Gly
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ENST00000579953.5:c.3281A>G
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ENSP00000463727.1:p.Glu1094Gly
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ENST00000580168.5:c.3281A>G
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ENSP00000464512.1:p.Glu1094Gly
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NM_014877.3:c.3278A>G
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NP_055692.2:p.Glu1093Gly
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XM_005257888.3:c.3359A>G
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XP_005257945.1:p.Glu1120Gly
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XM_005257889.3:c.3281A>G
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XP_005257946.1:p.Glu1094Gly
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XM_005257890.3:c.3257A>G
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XP_005257947.1:p.Glu1086Gly
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XM_006722214.2:c.3362A>G
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XP_006722277.1:p.Glu1121Gly
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XM_006722215.2:c.2657A>G
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XP_006722278.1:p.Glu886Gly
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XM_006722216.2:c.2186A>G
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XP_006722279.1:p.Glu729Gly
|
|
XM_011525544.1:c.3362A>G
|
XP_011523846.1:p.Glu1121Gly
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|
XM_011525545.1:c.3362A>G
|
XP_011523847.1:p.Glu1121Gly
|
|
XR_934629.1:n.3353A>G
|
|
|
NM_001330447.1:c.3281A>G
|
NP_001317376.1:p.Glu1094Gly
|
|
XM_005257888.5:c.3359A>G
|
XP_005257945.1:p.Glu1120Gly
|
|
XM_006722214.4:c.3362A>G
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XP_006722277.1:p.Glu1121Gly
|
|
XM_006722215.3:c.2657A>G
|
XP_006722278.1:p.Glu886Gly
|
|
XM_006722216.3:c.2186A>G
|
XP_006722279.1:p.Glu729Gly
|
|
XM_011525544.2:c.3362A>G
|
XP_011523846.1:p.Glu1121Gly
|
|
XM_017025477.2:c.2573A>G
|
XP_016880966.1:p.Glu858Gly
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|
XM_017025478.1:c.2105A>G
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XP_016880967.1:p.Glu702Gly
|
|
XR_001752712.2:n.3453A>G
|
|
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XR_001752713.2:n.3305A>G
|
|
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XR_001752714.2:n.3221A>G
|
|
|
NM_014877.4:c.3278A>G
MANE Select
|
NP_055692.3:p.Glu1093Gly
|
|
NM_001330447.2:c.3281A>G
|
NP_001317376.2:p.Glu1094Gly
|
|