ENST00000367698.4:c.977A>T
MANE Select
|
ENSP00000356671.3:p.Lys326Met
|
|
ENST00000367698.3:c.977A>T
|
ENSP00000356671.3:p.Lys326Met
|
|
ENST00000617423.4:c.559+2136A>T
|
ENSP00000478688.1:n.559+2136A>T
|
|
NM_000488.3:c.977A>T , LRG_577t1:c.977A>T
|
NP_000479.1:p.Lys326Met
|
|
XM_005245198.2:c.833A>T
|
XP_005245255.1:p.Lys278Met
|
|
NM_001365052.1:c.833A>T
|
NP_001351981.1:p.Lys278Met
|
|
NM_000488.4:c.977A>T
MANE Select
|
NP_000479.1:p.Lys326Met
|
|
NM_001365052.2:c.833A>T
|
NP_001351981.1:p.Lys278Met
|
|
NM_001386302.1:c.1100A>T
|
NP_001373231.1:p.Lys367Met
|
|
NM_001386303.1:c.1058A>T
|
NP_001373232.1:p.Lys353Met
|
|
NM_001386304.1:c.956A>T
|
NP_001373233.1:p.Lys319Met
|
|
NM_001386305.1:c.920A>T
|
NP_001373234.1:p.Lys307Met
|
|
NM_001386306.1:c.761A>T
|
NP_001373235.1:p.Lys254Met
|
|