ENST00000367698.4:c.1319T>G
MANE Select
|
ENSP00000356671.3:p.Phe440Cys
|
|
ENST00000367698.3:c.1319T>G
|
ENSP00000356671.3:p.Phe440Cys
|
|
ENST00000617423.4:c.704T>G
|
ENSP00000478688.1:p.Phe235Cys
|
|
NM_000488.3:c.1319T>G , LRG_577t1:c.1319T>G
|
NP_000479.1:p.Phe440Cys
|
|
XM_005245198.2:c.1175T>G
|
XP_005245255.1:p.Phe392Cys
|
|
NM_001365052.1:c.1175T>G
|
NP_001351981.1:p.Phe392Cys
|
|
NM_000488.4:c.1319T>G
MANE Select
|
NP_000479.1:p.Phe440Cys
|
|
NM_001365052.2:c.1175T>G
|
NP_001351981.1:p.Phe392Cys
|
|
NM_001386302.1:c.1442T>G
|
NP_001373231.1:p.Phe481Cys
|
|
NM_001386303.1:c.1400T>G
|
NP_001373232.1:p.Phe467Cys
|
|
NM_001386304.1:c.1298T>G
|
NP_001373233.1:p.Phe433Cys
|
|
NM_001386305.1:c.1262T>G
|
NP_001373234.1:p.Phe421Cys
|
|
NM_001386306.1:c.1103T>G
|
NP_001373235.1:p.Phe368Cys
|
|