|
ENST00000367698.4:c.868T=
MANE Select
|
ENSP00000356671.3:p.Phe290=
|
|
|
ENST00000367698.3:c.868T=
|
ENSP00000356671.3:p.Phe290=
|
|
|
ENST00000487183.1:n.519T=
|
|
|
|
ENST00000617423.4:c.559+2027T=
|
ENSP00000478688.1:n.559+2027T=
|
|
|
NM_000488.3:c.868T= , LRG_577t1:c.868T=
|
NP_000479.1:p.Phe290=
|
|
|
XM_005245198.2:c.724T=
|
XP_005245255.1:p.Phe242=
|
|
|
NM_001365052.1:c.724T=
|
NP_001351981.1:p.Phe242=
|
|
|
NM_000488.4:c.868T=
MANE Select
|
NP_000479.1:p.Phe290=
|
|
|
NM_001365052.2:c.724T=
|
NP_001351981.1:p.Phe242=
|
|
|
NM_001386302.1:c.991T=
|
NP_001373231.1:p.Phe331=
|
|
|
NM_001386303.1:c.949T=
|
NP_001373232.1:p.Phe317=
|
|
|
NM_001386304.1:c.847T=
|
NP_001373233.1:p.Phe283=
|
|
|
NM_001386305.1:c.811T=
|
NP_001373234.1:p.Phe271=
|
|
|
NM_001386306.1:c.652T=
|
NP_001373235.1:p.Phe218=
|
|
