ENST00000367698.4:c.1369A>T
MANE Select
|
ENSP00000356671.3:p.Arg457Ter
|
|
ENST00000367698.3:c.1369A>T
|
ENSP00000356671.3:p.Arg457Ter
|
|
ENST00000617423.4:c.754A>T
|
ENSP00000478688.1:p.Arg252Ter
|
|
NM_000488.3:c.1369A>T , LRG_577t1:c.1369A>T
|
NP_000479.1:p.Arg457Ter
|
|
XM_005245198.2:c.1225A>T
|
XP_005245255.1:p.Arg409Ter
|
|
NM_001365052.1:c.1225A>T
|
NP_001351981.1:p.Arg409Ter
|
|
NM_000488.4:c.1369A>T
MANE Select
|
NP_000479.1:p.Arg457Ter
|
|
NM_001365052.2:c.1225A>T
|
NP_001351981.1:p.Arg409Ter
|
|
NM_001386302.1:c.1492A>T
|
NP_001373231.1:p.Arg498Ter
|
|
NM_001386303.1:c.1450A>T
|
NP_001373232.1:p.Arg484Ter
|
|
NM_001386304.1:c.1348A>T
|
NP_001373233.1:p.Arg450Ter
|
|
NM_001386305.1:c.1312A>T
|
NP_001373234.1:p.Arg438Ter
|
|
NM_001386306.1:c.1153A>T
|
NP_001373235.1:p.Arg385Ter
|
|