ENST00000367698.4:c.1238A>C
MANE Select
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ENSP00000356671.3:p.Glu413Ala
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ENST00000367698.3:c.1238A>C
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ENSP00000356671.3:p.Glu413Ala
|
|
ENST00000617423.4:c.623A>C
|
ENSP00000478688.1:p.Glu208Ala
|
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NM_000488.3:c.1238A>C , LRG_577t1:c.1238A>C
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NP_000479.1:p.Glu413Ala
|
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XM_005245198.2:c.1094A>C
|
XP_005245255.1:p.Glu365Ala
|
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NM_001365052.1:c.1094A>C
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NP_001351981.1:p.Glu365Ala
|
|
NM_000488.4:c.1238A>C
MANE Select
|
NP_000479.1:p.Glu413Ala
|
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NM_001365052.2:c.1094A>C
|
NP_001351981.1:p.Glu365Ala
|
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NM_001386302.1:c.1361A>C
|
NP_001373231.1:p.Glu454Ala
|
|
NM_001386303.1:c.1319A>C
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NP_001373232.1:p.Glu440Ala
|
|
NM_001386304.1:c.1217A>C
|
NP_001373233.1:p.Glu406Ala
|
|
NM_001386305.1:c.1181A>C
|
NP_001373234.1:p.Glu394Ala
|
|
NM_001386306.1:c.1022A>C
|
NP_001373235.1:p.Glu341Ala
|
|