ENST00000367698.4:c.943C>T
MANE Select
|
ENSP00000356671.3:p.Leu315Phe
|
|
ENST00000367698.3:c.943C>T
|
ENSP00000356671.3:p.Leu315Phe
|
|
ENST00000487183.1:n.594C>T
|
|
|
ENST00000617423.4:c.559+2102C>T
|
ENSP00000478688.1:n.559+2102C>T
|
|
NM_000488.3:c.943C>T , LRG_577t1:c.943C>T
|
NP_000479.1:p.Leu315Phe
|
|
XM_005245198.2:c.799C>T
|
XP_005245255.1:p.Leu267Phe
|
|
NM_001365052.1:c.799C>T
|
NP_001351981.1:p.Leu267Phe
|
|
NM_000488.4:c.943C>T
MANE Select
|
NP_000479.1:p.Leu315Phe
|
|
NM_001365052.2:c.799C>T
|
NP_001351981.1:p.Leu267Phe
|
|
NM_001386302.1:c.1066C>T
|
NP_001373231.1:p.Leu356Phe
|
|
NM_001386303.1:c.1024C>T
|
NP_001373232.1:p.Leu342Phe
|
|
NM_001386304.1:c.922C>T
|
NP_001373233.1:p.Leu308Phe
|
|
NM_001386305.1:c.886C>T
|
NP_001373234.1:p.Leu296Phe
|
|
NM_001386306.1:c.727C>T
|
NP_001373235.1:p.Leu243Phe
|
|