ENST00000367698.4:c.1236T>A
MANE Select
|
ENSP00000356671.3:p.Ser412Arg
|
|
ENST00000367698.3:c.1236T>A
|
ENSP00000356671.3:p.Ser412Arg
|
|
ENST00000617423.4:c.621T>A
|
ENSP00000478688.1:p.Ser207Arg
|
|
NM_000488.3:c.1236T>A , LRG_577t1:c.1236T>A
|
NP_000479.1:p.Ser412Arg
|
|
XM_005245198.2:c.1092T>A
|
XP_005245255.1:p.Ser364Arg
|
|
NM_001365052.1:c.1092T>A
|
NP_001351981.1:p.Ser364Arg
|
|
NM_000488.4:c.1236T>A
MANE Select
|
NP_000479.1:p.Ser412Arg
|
|
NM_001365052.2:c.1092T>A
|
NP_001351981.1:p.Ser364Arg
|
|
NM_001386302.1:c.1359T>A
|
NP_001373231.1:p.Ser453Arg
|
|
NM_001386303.1:c.1317T>A
|
NP_001373232.1:p.Ser439Arg
|
|
NM_001386304.1:c.1215T>A
|
NP_001373233.1:p.Ser405Arg
|
|
NM_001386305.1:c.1179T>A
|
NP_001373234.1:p.Ser393Arg
|
|
NM_001386306.1:c.1020T>A
|
NP_001373235.1:p.Ser340Arg
|
|