|
ENST00000367698.4:c.780G=
MANE Select
|
ENSP00000356671.3:p.Lys260=
|
|
|
ENST00000367698.3:c.780G=
|
ENSP00000356671.3:p.Lys260=
|
|
|
ENST00000487183.1:n.431G=
|
|
|
|
ENST00000617423.4:c.559+1939G=
|
ENSP00000478688.1:n.559+1939G=
|
|
|
NM_000488.3:c.780G= , LRG_577t1:c.780G=
|
NP_000479.1:p.Lys260=
|
|
|
XM_005245198.2:c.636G=
|
XP_005245255.1:p.Lys212=
|
|
|
NM_001365052.1:c.636G=
|
NP_001351981.1:p.Lys212=
|
|
|
NM_000488.4:c.780G=
MANE Select
|
NP_000479.1:p.Lys260=
|
|
|
NM_001365052.2:c.636G=
|
NP_001351981.1:p.Lys212=
|
|
|
NM_001386302.1:c.903G=
|
NP_001373231.1:p.Lys301=
|
|
|
NM_001386303.1:c.861G=
|
NP_001373232.1:p.Lys287=
|
|
|
NM_001386304.1:c.759G=
|
NP_001373233.1:p.Lys253=
|
|
|
NM_001386305.1:c.763-40G=
|
NP_001373234.1:n.763-40G=
|
|
|
NM_001386306.1:c.564G=
|
NP_001373235.1:p.Lys188=
|
|
