ENST00000367698.4:c.961G=
MANE Select
|
ENSP00000356671.3:p.Glu321=
|
|
ENST00000367698.3:c.961G=
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ENSP00000356671.3:p.Glu321=
|
|
ENST00000487183.1:n.612G=
|
|
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ENST00000617423.4:c.559+2120G=
|
ENSP00000478688.1:n.559+2120G=
|
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NM_000488.3:c.961G= , LRG_577t1:c.961G=
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NP_000479.1:p.Glu321=
|
|
XM_005245198.2:c.817G=
|
XP_005245255.1:p.Glu273=
|
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NM_001365052.1:c.817G=
|
NP_001351981.1:p.Glu273=
|
|
NM_000488.4:c.961G=
MANE Select
|
NP_000479.1:p.Glu321=
|
|
NM_001365052.2:c.817G=
|
NP_001351981.1:p.Glu273=
|
|
NM_001386302.1:c.1084G=
|
NP_001373231.1:p.Glu362=
|
|
NM_001386303.1:c.1042G=
|
NP_001373232.1:p.Glu348=
|
|
NM_001386304.1:c.940G=
|
NP_001373233.1:p.Glu314=
|
|
NM_001386305.1:c.904G=
|
NP_001373234.1:p.Glu302=
|
|
NM_001386306.1:c.745G=
|
NP_001373235.1:p.Glu249=
|
|