|
ENST00000367698.4:c.784A>C
MANE Select
|
ENSP00000356671.3:p.Ser262Arg
|
|
|
ENST00000367698.3:c.784A>C
|
ENSP00000356671.3:p.Ser262Arg
|
|
|
ENST00000487183.1:n.435A>C
|
|
|
|
ENST00000617423.4:c.559+1943A>C
|
ENSP00000478688.1:n.559+1943A>C
|
|
|
NM_000488.3:c.784A>C , LRG_577t1:c.784A>C
|
NP_000479.1:p.Ser262Arg
|
|
|
XM_005245198.2:c.640A>C
|
XP_005245255.1:p.Ser214Arg
|
|
|
NM_001365052.1:c.640A>C
|
NP_001351981.1:p.Ser214Arg
|
|
|
NM_000488.4:c.784A>C
MANE Select
|
NP_000479.1:p.Ser262Arg
|
|
|
NM_001365052.2:c.640A>C
|
NP_001351981.1:p.Ser214Arg
|
|
|
NM_001386302.1:c.907A>C
|
NP_001373231.1:p.Ser303Arg
|
|
|
NM_001386303.1:c.865A>C
|
NP_001373232.1:p.Ser289Arg
|
|
|
NM_001386304.1:c.763A>C
|
NP_001373233.1:p.Ser255Arg
|
|
|
NM_001386305.1:c.763-36A>C
|
NP_001373234.1:n.763-36A>C
|
|
|
NM_001386306.1:c.568A>C
|
NP_001373235.1:p.Ser190Arg
|
|
