ENST00000270301.12:c.3139A>G
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ENSP00000270301.6:p.Ser1047Gly
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ENST00000401500.7:c.3139A>G
MANE Select
|
ENSP00000384792.1:p.Ser1047Gly
|
|
ENST00000587391.6:c.*2414A>G
|
ENSP00000465525.1:n.*2414A>G
|
|
ENST00000679357.1:c.929A>G
|
|
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ENST00000679422.1:c.818A>G
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|
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ENST00000679682.1:c.3124A>G
|
ENSP00000506226.1:p.Ser1042Gly
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ENST00000679714.1:c.3133A>G
|
ENSP00000506627.1:p.Ser1045Gly
|
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ENST00000679757.1:c.2788A>G
|
ENSP00000505158.1:p.Ser930Gly
|
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ENST00000679858.1:c.*2521A>G
|
ENSP00000505655.1:n.*2521A>G
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ENST00000680211.1:c.-261A>G
|
ENSP00000506102.1:n.-261A>G
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ENST00000680349.1:n.1122A>G
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|
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ENST00000680403.1:c.3139A>G
|
ENSP00000505677.1:p.Ser1047Gly
|
|
ENST00000680564.1:c.2972-667A>G
|
ENSP00000505582.1:n.2972-667A>G
|
|
ENST00000680590.1:c.*1534A>G
|
ENSP00000505350.1:n.*1534A>G
|
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ENST00000680739.1:c.57A>G
|
|
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ENST00000680773.1:n.1055A>G
|
|
|
ENST00000680806.1:c.*1857A>G
|
ENSP00000506418.1:n.*1857A>G
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|
ENST00000680997.1:n.486A>G
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|
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ENST00000681088.1:c.801A>G
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ENST00000681608.1:n.87A>G
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|
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ENST00000681625.1:c.*471A>G
|
ENSP00000505555.1:n.*471A>G
|
|
ENST00000270301.11:c.3139A>G
|
ENSP00000270301.6:p.Ser1047Gly
|
|
ENST00000401500.6:c.3139A>G
|
ENSP00000384792.1:p.Ser1047Gly
|
|
ENST00000587391.5:c.*2414A>G
|
ENSP00000465525.1:n.*2414A>G
|
|
NM_001083961.1:c.3139A>G
|
NP_001077430.1:p.Ser1047Gly
|
|
NM_173636.4:c.3139A>G
|
NP_775907.4:p.Ser1047Gly
|
|
XM_005258809.2:c.3028A>G
|
XP_005258866.1:p.Ser1010Gly
|
|
XM_011526837.1:c.3124A>G
|
XP_011525139.1:p.Ser1042Gly
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|
XM_011526838.1:c.2972-667A>G
|
XP_011525140.1:n.2972-667A>G
|
|
XM_011526839.1:c.2788A>G
|
XP_011525141.1:p.Ser930Gly
|
|
XM_011526840.1:c.2131A>G
|
XP_011525142.1:p.Ser711Gly
|
|
XM_011526841.1:c.1717A>G
|
XP_011525143.1:p.Ser573Gly
|
|
XM_011526842.1:c.1570A>G
|
XP_011525144.1:p.Ser524Gly
|
|
XM_011526843.1:c.886A>G
|
XP_011525145.1:p.Ser296Gly
|
|
XM_011526844.1:c.886A>G
|
XP_011525146.1:p.Ser296Gly
|
|
XM_011526840.2:c.2131A>G
|
XP_011525142.1:p.Ser711Gly
|
|
XM_011526841.2:c.1717A>G
|
XP_011525143.1:p.Ser573Gly
|
|
XM_011526844.2:c.886A>G
|
XP_011525146.1:p.Ser296Gly
|
|
XM_017026665.1:c.3139A>G
|
XP_016882154.1:p.Ser1047Gly
|
|
NM_001083961.2:c.3139A>G
MANE Select
|
NP_001077430.1:p.Ser1047Gly
|
|
NM_173636.5:c.3139A>G
|
NP_775907.4:p.Ser1047Gly
|
|