ENST00000367698.4:c.1387G>A
MANE Select
|
ENSP00000356671.3:p.Val463Ile
|
|
ENST00000367698.3:c.1387G>A
|
ENSP00000356671.3:p.Val463Ile
|
|
ENST00000617423.4:c.772G>A
|
ENSP00000478688.1:p.Val258Ile
|
|
NM_000488.3:c.1387G>A , LRG_577t1:c.1387G>A
|
NP_000479.1:p.Val463Ile
|
|
XM_005245198.2:c.1243G>A
|
XP_005245255.1:p.Val415Ile
|
|
NM_001365052.1:c.1243G>A
|
NP_001351981.1:p.Val415Ile
|
|
NM_000488.4:c.1387G>A
MANE Select
|
NP_000479.1:p.Val463Ile
|
|
NM_001365052.2:c.1243G>A
|
NP_001351981.1:p.Val415Ile
|
|
NM_001386302.1:c.1510G>A
|
NP_001373231.1:p.Val504Ile
|
|
NM_001386303.1:c.1468G>A
|
NP_001373232.1:p.Val490Ile
|
|
NM_001386304.1:c.1366G>A
|
NP_001373233.1:p.Val456Ile
|
|
NM_001386305.1:c.1330G>A
|
NP_001373234.1:p.Val444Ile
|
|
NM_001386306.1:c.1171G>A
|
NP_001373235.1:p.Val391Ile
|
|