ENST00000367698.4:c.1125G>C
MANE Select
|
ENSP00000356671.3:p.Leu375=
|
|
ENST00000367698.3:c.1125G>C
|
ENSP00000356671.3:p.Leu375=
|
|
ENST00000617423.4:c.560-2087G>C
|
ENSP00000478688.1:n.560-2087G>C
|
|
NM_000488.3:c.1125G>C , LRG_577t1:c.1125G>C
|
NP_000479.1:p.Leu375=
|
|
XM_005245198.2:c.981G>C
|
XP_005245255.1:p.Leu327=
|
|
NM_001365052.1:c.981G>C
|
NP_001351981.1:p.Leu327=
|
|
NM_000488.4:c.1125G>C
MANE Select
|
NP_000479.1:p.Leu375=
|
|
NM_001365052.2:c.981G>C
|
NP_001351981.1:p.Leu327=
|
|
NM_001386302.1:c.1248G>C
|
NP_001373231.1:p.Leu416=
|
|
NM_001386303.1:c.1206G>C
|
NP_001373232.1:p.Leu402=
|
|
NM_001386304.1:c.1104G>C
|
NP_001373233.1:p.Leu368=
|
|
NM_001386305.1:c.1068G>C
|
NP_001373234.1:p.Leu356=
|
|
NM_001386306.1:c.909G>C
|
NP_001373235.1:p.Leu303=
|
|