ENST00000367698.4:c.1025A>T
MANE Select
|
ENSP00000356671.3:p.Glu342Val
|
|
ENST00000367698.3:c.1025A>T
|
ENSP00000356671.3:p.Glu342Val
|
|
ENST00000617423.4:c.559+2184A>T
|
ENSP00000478688.1:n.559+2184A>T
|
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NM_000488.3:c.1025A>T , LRG_577t1:c.1025A>T
|
NP_000479.1:p.Glu342Val
|
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XM_005245198.2:c.881A>T
|
XP_005245255.1:p.Glu294Val
|
|
NM_001365052.1:c.881A>T
|
NP_001351981.1:p.Glu294Val
|
|
NM_000488.4:c.1025A>T
MANE Select
|
NP_000479.1:p.Glu342Val
|
|
NM_001365052.2:c.881A>T
|
NP_001351981.1:p.Glu294Val
|
|
NM_001386302.1:c.1148A>T
|
NP_001373231.1:p.Glu383Val
|
|
NM_001386303.1:c.1106A>T
|
NP_001373232.1:p.Glu369Val
|
|
NM_001386304.1:c.1004A>T
|
NP_001373233.1:p.Glu335Val
|
|
NM_001386305.1:c.968A>T
|
NP_001373234.1:p.Glu323Val
|
|
NM_001386306.1:c.809A>T
|
NP_001373235.1:p.Glu270Val
|
|