ENST00000367698.4:c.1053C=
MANE Select
|
ENSP00000356671.3:p.His351=
|
|
ENST00000367698.3:c.1053C=
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ENSP00000356671.3:p.His351=
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|
ENST00000617423.4:c.560-2159C=
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ENSP00000478688.1:n.560-2159C=
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NM_000488.3:c.1053C= , LRG_577t1:c.1053C=
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NP_000479.1:p.His351=
|
|
XM_005245198.2:c.909C=
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XP_005245255.1:p.His303=
|
|
NM_001365052.1:c.909C=
|
NP_001351981.1:p.His303=
|
|
NM_000488.4:c.1053C=
MANE Select
|
NP_000479.1:p.His351=
|
|
NM_001365052.2:c.909C=
|
NP_001351981.1:p.His303=
|
|
NM_001386302.1:c.1176C=
|
NP_001373231.1:p.His392=
|
|
NM_001386303.1:c.1134C=
|
NP_001373232.1:p.His378=
|
|
NM_001386304.1:c.1032C=
|
NP_001373233.1:p.His344=
|
|
NM_001386305.1:c.996C=
|
NP_001373234.1:p.His332=
|
|
NM_001386306.1:c.837C=
|
NP_001373235.1:p.His279=
|
|