|
ENST00000367698.4:c.779A>T
MANE Select
|
ENSP00000356671.3:p.Lys260Met
|
|
|
ENST00000367698.3:c.779A>T
|
ENSP00000356671.3:p.Lys260Met
|
|
|
ENST00000487183.1:n.430A>T
|
|
|
|
ENST00000617423.4:c.559+1938A>T
|
ENSP00000478688.1:n.559+1938A>T
|
|
|
NM_000488.3:c.779A>T , LRG_577t1:c.779A>T
|
NP_000479.1:p.Lys260Met
|
|
|
XM_005245198.2:c.635A>T
|
XP_005245255.1:p.Lys212Met
|
|
|
NM_001365052.1:c.635A>T
|
NP_001351981.1:p.Lys212Met
|
|
|
NM_000488.4:c.779A>T
MANE Select
|
NP_000479.1:p.Lys260Met
|
|
|
NM_001365052.2:c.635A>T
|
NP_001351981.1:p.Lys212Met
|
|
|
NM_001386302.1:c.902A>T
|
NP_001373231.1:p.Lys301Met
|
|
|
NM_001386303.1:c.860A>T
|
NP_001373232.1:p.Lys287Met
|
|
|
NM_001386304.1:c.758A>T
|
NP_001373233.1:p.Lys253Met
|
|
|
NM_001386305.1:c.763-41A>T
|
NP_001373234.1:n.763-41A>T
|
|
|
NM_001386306.1:c.563A>T
|
NP_001373235.1:p.Lys188Met
|
|
