ENST00000367698.4:c.774G=
MANE Select
|
ENSP00000356671.3:p.Lys258=
|
|
ENST00000367698.3:c.774G=
|
ENSP00000356671.3:p.Lys258=
|
|
ENST00000487183.1:n.425G=
|
|
|
ENST00000617423.4:c.559+1933G=
|
ENSP00000478688.1:n.559+1933G=
|
|
NM_000488.3:c.774G= , LRG_577t1:c.774G=
|
NP_000479.1:p.Lys258=
|
|
XM_005245198.2:c.630G=
|
XP_005245255.1:p.Lys210=
|
|
NM_001365052.1:c.630G=
|
NP_001351981.1:p.Lys210=
|
|
NM_000488.4:c.774G=
MANE Select
|
NP_000479.1:p.Lys258=
|
|
NM_001365052.2:c.630G=
|
NP_001351981.1:p.Lys210=
|
|
NM_001386302.1:c.897G=
|
NP_001373231.1:p.Lys299=
|
|
NM_001386303.1:c.855G=
|
NP_001373232.1:p.Lys285=
|
|
NM_001386304.1:c.753G=
|
NP_001373233.1:p.Lys251=
|
|
NM_001386305.1:c.763-46G=
|
NP_001373234.1:n.763-46G=
|
|
NM_001386306.1:c.558G=
|
NP_001373235.1:p.Lys186=
|
|