ENST00000367698.4:c.852G>A
MANE Select
|
ENSP00000356671.3:p.Met284Ile
|
|
ENST00000367698.3:c.852G>A
|
ENSP00000356671.3:p.Met284Ile
|
|
ENST00000487183.1:n.503G>A
|
|
|
ENST00000617423.4:c.559+2011G>A
|
ENSP00000478688.1:n.559+2011G>A
|
|
NM_000488.3:c.852G>A , LRG_577t1:c.852G>A
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NP_000479.1:p.Met284Ile
|
|
XM_005245198.2:c.708G>A
|
XP_005245255.1:p.Met236Ile
|
|
NM_001365052.1:c.708G>A
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NP_001351981.1:p.Met236Ile
|
|
NM_000488.4:c.852G>A
MANE Select
|
NP_000479.1:p.Met284Ile
|
|
NM_001365052.2:c.708G>A
|
NP_001351981.1:p.Met236Ile
|
|
NM_001386302.1:c.975G>A
|
NP_001373231.1:p.Met325Ile
|
|
NM_001386303.1:c.933G>A
|
NP_001373232.1:p.Met311Ile
|
|
NM_001386304.1:c.831G>A
|
NP_001373233.1:p.Met277Ile
|
|
NM_001386305.1:c.795G>A
|
NP_001373234.1:p.Met265Ile
|
|
NM_001386306.1:c.636G>A
|
NP_001373235.1:p.Met212Ile
|
|