ENST00000367698.4:c.1012G>A
MANE Select
|
ENSP00000356671.3:p.Glu338Lys
|
|
ENST00000367698.3:c.1012G>A
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ENSP00000356671.3:p.Glu338Lys
|
|
ENST00000617423.4:c.559+2171G>A
|
ENSP00000478688.1:n.559+2171G>A
|
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NM_000488.3:c.1012G>A , LRG_577t1:c.1012G>A
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NP_000479.1:p.Glu338Lys
|
|
XM_005245198.2:c.868G>A
|
XP_005245255.1:p.Glu290Lys
|
|
NM_001365052.1:c.868G>A
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NP_001351981.1:p.Glu290Lys
|
|
NM_000488.4:c.1012G>A
MANE Select
|
NP_000479.1:p.Glu338Lys
|
|
NM_001365052.2:c.868G>A
|
NP_001351981.1:p.Glu290Lys
|
|
NM_001386302.1:c.1135G>A
|
NP_001373231.1:p.Glu379Lys
|
|
NM_001386303.1:c.1093G>A
|
NP_001373232.1:p.Glu365Lys
|
|
NM_001386304.1:c.991G>A
|
NP_001373233.1:p.Glu331Lys
|
|
NM_001386305.1:c.955G>A
|
NP_001373234.1:p.Glu319Lys
|
|
NM_001386306.1:c.796G>A
|
NP_001373235.1:p.Glu266Lys
|
|