ENST00000367698.4:c.893G>A
MANE Select
|
ENSP00000356671.3:p.Gly298Asp
|
|
ENST00000367698.3:c.893G>A
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ENSP00000356671.3:p.Gly298Asp
|
|
ENST00000487183.1:n.544G>A
|
|
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ENST00000617423.4:c.559+2052G>A
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ENSP00000478688.1:n.559+2052G>A
|
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NM_000488.3:c.893G>A , LRG_577t1:c.893G>A
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NP_000479.1:p.Gly298Asp
|
|
XM_005245198.2:c.749G>A
|
XP_005245255.1:p.Gly250Asp
|
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NM_001365052.1:c.749G>A
|
NP_001351981.1:p.Gly250Asp
|
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NM_000488.4:c.893G>A
MANE Select
|
NP_000479.1:p.Gly298Asp
|
|
NM_001365052.2:c.749G>A
|
NP_001351981.1:p.Gly250Asp
|
|
NM_001386302.1:c.1016G>A
|
NP_001373231.1:p.Gly339Asp
|
|
NM_001386303.1:c.974G>A
|
NP_001373232.1:p.Gly325Asp
|
|
NM_001386304.1:c.872G>A
|
NP_001373233.1:p.Gly291Asp
|
|
NM_001386305.1:c.836G>A
|
NP_001373234.1:p.Gly279Asp
|
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NM_001386306.1:c.677G>A
|
NP_001373235.1:p.Gly226Asp
|
|