ENST00000367698.4:c.854A>T
MANE Select
|
ENSP00000356671.3:p.Tyr285Phe
|
|
ENST00000367698.3:c.854A>T
|
ENSP00000356671.3:p.Tyr285Phe
|
|
ENST00000487183.1:n.505A>T
|
|
|
ENST00000617423.4:c.559+2013A>T
|
ENSP00000478688.1:n.559+2013A>T
|
|
NM_000488.3:c.854A>T , LRG_577t1:c.854A>T
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NP_000479.1:p.Tyr285Phe
|
|
XM_005245198.2:c.710A>T
|
XP_005245255.1:p.Tyr237Phe
|
|
NM_001365052.1:c.710A>T
|
NP_001351981.1:p.Tyr237Phe
|
|
NM_000488.4:c.854A>T
MANE Select
|
NP_000479.1:p.Tyr285Phe
|
|
NM_001365052.2:c.710A>T
|
NP_001351981.1:p.Tyr237Phe
|
|
NM_001386302.1:c.977A>T
|
NP_001373231.1:p.Tyr326Phe
|
|
NM_001386303.1:c.935A>T
|
NP_001373232.1:p.Tyr312Phe
|
|
NM_001386304.1:c.833A>T
|
NP_001373233.1:p.Tyr278Phe
|
|
NM_001386305.1:c.797A>T
|
NP_001373234.1:p.Tyr266Phe
|
|
NM_001386306.1:c.638A>T
|
NP_001373235.1:p.Tyr213Phe
|
|