ENST00000367698.4:c.1127T>G
MANE Select
|
ENSP00000356671.3:p.Phe376Cys
|
|
ENST00000367698.3:c.1127T>G
|
ENSP00000356671.3:p.Phe376Cys
|
|
ENST00000617423.4:c.560-2085T>G
|
ENSP00000478688.1:n.560-2085T>G
|
|
NM_000488.3:c.1127T>G , LRG_577t1:c.1127T>G
|
NP_000479.1:p.Phe376Cys
|
|
XM_005245198.2:c.983T>G
|
XP_005245255.1:p.Phe328Cys
|
|
NM_001365052.1:c.983T>G
|
NP_001351981.1:p.Phe328Cys
|
|
NM_000488.4:c.1127T>G
MANE Select
|
NP_000479.1:p.Phe376Cys
|
|
NM_001365052.2:c.983T>G
|
NP_001351981.1:p.Phe328Cys
|
|
NM_001386302.1:c.1250T>G
|
NP_001373231.1:p.Phe417Cys
|
|
NM_001386303.1:c.1208T>G
|
NP_001373232.1:p.Phe403Cys
|
|
NM_001386304.1:c.1106T>G
|
NP_001373233.1:p.Phe369Cys
|
|
NM_001386305.1:c.1070T>G
|
NP_001373234.1:p.Phe357Cys
|
|
NM_001386306.1:c.911T>G
|
NP_001373235.1:p.Phe304Cys
|
|