|
ENST00000367698.4:c.834G>C
MANE Select
|
ENSP00000356671.3:p.Ser278=
|
|
|
ENST00000367698.3:c.834G>C
|
ENSP00000356671.3:p.Ser278=
|
|
|
ENST00000487183.1:n.485G>C
|
|
|
|
ENST00000617423.4:c.559+1993G>C
|
ENSP00000478688.1:n.559+1993G>C
|
|
|
NM_000488.3:c.834G>C , LRG_577t1:c.834G>C
|
NP_000479.1:p.Ser278=
|
|
|
XM_005245198.2:c.690G>C
|
XP_005245255.1:p.Ser230=
|
|
|
NM_001365052.1:c.690G>C
|
NP_001351981.1:p.Ser230=
|
|
|
NM_000488.4:c.834G>C
MANE Select
|
NP_000479.1:p.Ser278=
|
|
|
NM_001365052.2:c.690G>C
|
NP_001351981.1:p.Ser230=
|
|
|
NM_001386302.1:c.957G>C
|
NP_001373231.1:p.Ser319=
|
|
|
NM_001386303.1:c.915G>C
|
NP_001373232.1:p.Ser305=
|
|
|
NM_001386304.1:c.813G>C
|
NP_001373233.1:p.Ser271=
|
|
|
NM_001386305.1:c.777G>C
|
NP_001373234.1:p.Ser259=
|
|
|
NM_001386306.1:c.618G>C
|
NP_001373235.1:p.Ser206=
|
|
