ENST00000367698.4:c.1089G>T
MANE Select
|
ENSP00000356671.3:p.Leu363Phe
|
|
ENST00000367698.3:c.1089G>T
|
ENSP00000356671.3:p.Leu363Phe
|
|
ENST00000617423.4:c.560-2123G>T
|
ENSP00000478688.1:n.560-2123G>T
|
|
NM_000488.3:c.1089G>T , LRG_577t1:c.1089G>T
|
NP_000479.1:p.Leu363Phe
|
|
XM_005245198.2:c.945G>T
|
XP_005245255.1:p.Leu315Phe
|
|
NM_001365052.1:c.945G>T
|
NP_001351981.1:p.Leu315Phe
|
|
NM_000488.4:c.1089G>T
MANE Select
|
NP_000479.1:p.Leu363Phe
|
|
NM_001365052.2:c.945G>T
|
NP_001351981.1:p.Leu315Phe
|
|
NM_001386302.1:c.1212G>T
|
NP_001373231.1:p.Leu404Phe
|
|
NM_001386303.1:c.1170G>T
|
NP_001373232.1:p.Leu390Phe
|
|
NM_001386304.1:c.1068G>T
|
NP_001373233.1:p.Leu356Phe
|
|
NM_001386305.1:c.1032G>T
|
NP_001373234.1:p.Leu344Phe
|
|
NM_001386306.1:c.873G>T
|
NP_001373235.1:p.Leu291Phe
|
|