ENST00000330889.8:c.1052A>C
MANE Select
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ENSP00000329468.3:p.Glu351Ala
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ENST00000330889.7:c.1052A>C
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ENSP00000329468.3:p.Glu351Ala
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ENST00000470962.1:n.472A>C
|
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ENST00000480980.1:n.486A>C
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ENST00000580525.5:c.1070A>C
|
ENSP00000464121.1:p.Glu357Ala
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ENST00000581285.5:c.968A>C
|
ENSP00000464155.1:p.Glu323Ala
|
|
ENST00000584828.5:c.402+19A>C
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ENST00000585130.5:c.*651A>C
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ENSP00000464120.1:n.*651A>C
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NM_018404.2:c.1052A>C
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NP_060874.1:p.Glu351Ala
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XM_005258008.2:c.1070A>C
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XP_005258065.1:p.Glu357Ala
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XM_005258011.2:c.1007A>C
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XP_005258068.1:p.Glu336Ala
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XM_006721973.2:c.1051+19A>C
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XP_006722036.1:n.1051+19A>C
|
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XM_011524993.1:c.1067A>C
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XP_011523295.1:p.Glu356Ala
|
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XM_011524994.1:c.1049A>C
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XP_011523296.1:p.Glu350Ala
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NM_001346712.1:c.1070A>C
|
NP_001333641.1:p.Glu357Ala
|
|
NM_001346714.1:c.1049A>C
|
NP_001333643.1:p.Glu350Ala
|
|
NM_001346716.1:c.1033+19A>C
|
NP_001333645.1:n.1033+19A>C
|
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NR_144488.1:n.1251A>C
|
|
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XM_024450831.1:c.1052A>C
|
XP_024306599.1:p.Glu351Ala
|
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XM_024450832.1:c.1067A>C
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XP_024306600.1:p.Glu356Ala
|
|
XM_024450833.1:c.1007A>C
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XP_024306601.1:p.Glu336Ala
|
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XM_024450834.1:c.1051+19A>C
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XP_024306602.1:n.1051+19A>C
|
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XM_024450835.1:c.686A>C
|
XP_024306603.1:p.Glu229Ala
|
|
NM_018404.3:c.1052A>C
MANE Select
|
NP_060874.1:p.Glu351Ala
|
|
NM_001346712.2:c.1070A>C
|
NP_001333641.1:p.Glu357Ala
|
|
NM_001346714.2:c.1049A>C
|
NP_001333643.1:p.Glu350Ala
|
|
NM_001346716.2:c.1033+19A>C
|
NP_001333645.1:n.1033+19A>C
|
|
NR_144488.2:n.1042A>C
|
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