ENST00000367698.4:c.1084A=
MANE Select
|
ENSP00000356671.3:p.Ser362=
|
|
ENST00000367698.3:c.1084A=
|
ENSP00000356671.3:p.Ser362=
|
|
ENST00000617423.4:c.560-2128A=
|
ENSP00000478688.1:n.560-2128A=
|
|
NM_000488.3:c.1084A= , LRG_577t1:c.1084A=
|
NP_000479.1:p.Ser362=
|
|
XM_005245198.2:c.940A=
|
XP_005245255.1:p.Ser314=
|
|
NM_001365052.1:c.940A=
|
NP_001351981.1:p.Ser314=
|
|
NM_000488.4:c.1084A=
MANE Select
|
NP_000479.1:p.Ser362=
|
|
NM_001365052.2:c.940A=
|
NP_001351981.1:p.Ser314=
|
|
NM_001386302.1:c.1207A=
|
NP_001373231.1:p.Ser403=
|
|
NM_001386303.1:c.1165A=
|
NP_001373232.1:p.Ser389=
|
|
NM_001386304.1:c.1063A=
|
NP_001373233.1:p.Ser355=
|
|
NM_001386305.1:c.1027A=
|
NP_001373234.1:p.Ser343=
|
|
NM_001386306.1:c.868A=
|
NP_001373235.1:p.Ser290=
|
|