ENST00000367698.4:c.781T>C
MANE Select
|
ENSP00000356671.3:p.Phe261Leu
|
|
ENST00000367698.3:c.781T>C
|
ENSP00000356671.3:p.Phe261Leu
|
|
ENST00000487183.1:n.432T>C
|
|
|
ENST00000617423.4:c.559+1940T>C
|
ENSP00000478688.1:n.559+1940T>C
|
|
NM_000488.3:c.781T>C , LRG_577t1:c.781T>C
|
NP_000479.1:p.Phe261Leu
|
|
XM_005245198.2:c.637T>C
|
XP_005245255.1:p.Phe213Leu
|
|
NM_001365052.1:c.637T>C
|
NP_001351981.1:p.Phe213Leu
|
|
NM_000488.4:c.781T>C
MANE Select
|
NP_000479.1:p.Phe261Leu
|
|
NM_001365052.2:c.637T>C
|
NP_001351981.1:p.Phe213Leu
|
|
NM_001386302.1:c.904T>C
|
NP_001373231.1:p.Phe302Leu
|
|
NM_001386303.1:c.862T>C
|
NP_001373232.1:p.Phe288Leu
|
|
NM_001386304.1:c.760T>C
|
NP_001373233.1:p.Phe254Leu
|
|
NM_001386305.1:c.763-39T>C
|
NP_001373234.1:n.763-39T>C
|
|
NM_001386306.1:c.565T>C
|
NP_001373235.1:p.Phe189Leu
|
|