ENST00000367698.4:c.1336G>T
MANE Select
|
ENSP00000356671.3:p.Glu446Ter
|
|
ENST00000367698.3:c.1336G>T
|
ENSP00000356671.3:p.Glu446Ter
|
|
ENST00000617423.4:c.721G>T
|
ENSP00000478688.1:p.Glu241Ter
|
|
NM_000488.3:c.1336G>T , LRG_577t1:c.1336G>T
|
NP_000479.1:p.Glu446Ter
|
|
XM_005245198.2:c.1192G>T
|
XP_005245255.1:p.Glu398Ter
|
|
NM_001365052.1:c.1192G>T
|
NP_001351981.1:p.Glu398Ter
|
|
NM_000488.4:c.1336G>T
MANE Select
|
NP_000479.1:p.Glu446Ter
|
|
NM_001365052.2:c.1192G>T
|
NP_001351981.1:p.Glu398Ter
|
|
NM_001386302.1:c.1459G>T
|
NP_001373231.1:p.Glu487Ter
|
|
NM_001386303.1:c.1417G>T
|
NP_001373232.1:p.Glu473Ter
|
|
NM_001386304.1:c.1315G>T
|
NP_001373233.1:p.Glu439Ter
|
|
NM_001386305.1:c.1279G>T
|
NP_001373234.1:p.Glu427Ter
|
|
NM_001386306.1:c.1120G>T
|
NP_001373235.1:p.Glu374Ter
|
|