ENST00000367698.4:c.868T>G
MANE Select
|
ENSP00000356671.3:p.Phe290Val
|
|
ENST00000367698.3:c.868T>G
|
ENSP00000356671.3:p.Phe290Val
|
|
ENST00000487183.1:n.519T>G
|
|
|
ENST00000617423.4:c.559+2027T>G
|
ENSP00000478688.1:n.559+2027T>G
|
|
NM_000488.3:c.868T>G , LRG_577t1:c.868T>G
|
NP_000479.1:p.Phe290Val
|
|
XM_005245198.2:c.724T>G
|
XP_005245255.1:p.Phe242Val
|
|
NM_001365052.1:c.724T>G
|
NP_001351981.1:p.Phe242Val
|
|
NM_000488.4:c.868T>G
MANE Select
|
NP_000479.1:p.Phe290Val
|
|
NM_001365052.2:c.724T>G
|
NP_001351981.1:p.Phe242Val
|
|
NM_001386302.1:c.991T>G
|
NP_001373231.1:p.Phe331Val
|
|
NM_001386303.1:c.949T>G
|
NP_001373232.1:p.Phe317Val
|
|
NM_001386304.1:c.847T>G
|
NP_001373233.1:p.Phe283Val
|
|
NM_001386305.1:c.811T>G
|
NP_001373234.1:p.Phe271Val
|
|
NM_001386306.1:c.652T>G
|
NP_001373235.1:p.Phe218Val
|
|