ENST00000367698.4:c.1370G>T
MANE Select
|
ENSP00000356671.3:p.Arg457Ile
|
|
ENST00000367698.3:c.1370G>T
|
ENSP00000356671.3:p.Arg457Ile
|
|
ENST00000617423.4:c.755G>T
|
ENSP00000478688.1:p.Arg252Ile
|
|
NM_000488.3:c.1370G>T , LRG_577t1:c.1370G>T
|
NP_000479.1:p.Arg457Ile
|
|
XM_005245198.2:c.1226G>T
|
XP_005245255.1:p.Arg409Ile
|
|
NM_001365052.1:c.1226G>T
|
NP_001351981.1:p.Arg409Ile
|
|
NM_000488.4:c.1370G>T
MANE Select
|
NP_000479.1:p.Arg457Ile
|
|
NM_001365052.2:c.1226G>T
|
NP_001351981.1:p.Arg409Ile
|
|
NM_001386302.1:c.1493G>T
|
NP_001373231.1:p.Arg498Ile
|
|
NM_001386303.1:c.1451G>T
|
NP_001373232.1:p.Arg484Ile
|
|
NM_001386304.1:c.1349G>T
|
NP_001373233.1:p.Arg450Ile
|
|
NM_001386305.1:c.1313G>T
|
NP_001373234.1:p.Arg438Ile
|
|
NM_001386306.1:c.1154G>T
|
NP_001373235.1:p.Arg385Ile
|
|