ENST00000367698.4:c.849G>A
MANE Select
|
ENSP00000356671.3:p.Met283Ile
|
|
ENST00000367698.3:c.849G>A
|
ENSP00000356671.3:p.Met283Ile
|
|
ENST00000487183.1:n.500G>A
|
|
|
ENST00000617423.4:c.559+2008G>A
|
ENSP00000478688.1:n.559+2008G>A
|
|
NM_000488.3:c.849G>A , LRG_577t1:c.849G>A
|
NP_000479.1:p.Met283Ile
|
|
XM_005245198.2:c.705G>A
|
XP_005245255.1:p.Met235Ile
|
|
NM_001365052.1:c.705G>A
|
NP_001351981.1:p.Met235Ile
|
|
NM_000488.4:c.849G>A
MANE Select
|
NP_000479.1:p.Met283Ile
|
|
NM_001365052.2:c.705G>A
|
NP_001351981.1:p.Met235Ile
|
|
NM_001386302.1:c.972G>A
|
NP_001373231.1:p.Met324Ile
|
|
NM_001386303.1:c.930G>A
|
NP_001373232.1:p.Met310Ile
|
|
NM_001386304.1:c.828G>A
|
NP_001373233.1:p.Met276Ile
|
|
NM_001386305.1:c.792G>A
|
NP_001373234.1:p.Met264Ile
|
|
NM_001386306.1:c.633G>A
|
NP_001373235.1:p.Met211Ile
|
|