|
ENST00000367698.4:c.1131C>T
MANE Select
|
ENSP00000356671.3:p.Ser377=
|
|
|
ENST00000367698.3:c.1131C>T
|
ENSP00000356671.3:p.Ser377=
|
|
|
ENST00000617423.4:c.560-2081C>T
|
ENSP00000478688.1:n.560-2081C>T
|
|
|
NM_000488.3:c.1131C>T , LRG_577t1:c.1131C>T
|
NP_000479.1:p.Ser377=
|
|
|
XM_005245198.2:c.987C>T
|
XP_005245255.1:p.Ser329=
|
|
|
NM_001365052.1:c.987C>T
|
NP_001351981.1:p.Ser329=
|
|
|
NM_000488.4:c.1131C>T
MANE Select
|
NP_000479.1:p.Ser377=
|
|
|
NM_001365052.2:c.987C>T
|
NP_001351981.1:p.Ser329=
|
|
|
NM_001386302.1:c.1254C>T
|
NP_001373231.1:p.Ser418=
|
|
|
NM_001386303.1:c.1212C>T
|
NP_001373232.1:p.Ser404=
|
|
|
NM_001386304.1:c.1110C>T
|
NP_001373233.1:p.Ser370=
|
|
|
NM_001386305.1:c.1074C>T
|
NP_001373234.1:p.Ser358=
|
|
|
NM_001386306.1:c.915C>T
|
NP_001373235.1:p.Ser305=
|
|
