ENST00000367698.4:c.885G=
MANE Select
|
ENSP00000356671.3:p.Val295=
|
|
ENST00000367698.3:c.885G=
|
ENSP00000356671.3:p.Val295=
|
|
ENST00000487183.1:n.536G=
|
|
|
ENST00000617423.4:c.559+2044G=
|
ENSP00000478688.1:n.559+2044G=
|
|
NM_000488.3:c.885G= , LRG_577t1:c.885G=
|
NP_000479.1:p.Val295=
|
|
XM_005245198.2:c.741G=
|
XP_005245255.1:p.Val247=
|
|
NM_001365052.1:c.741G=
|
NP_001351981.1:p.Val247=
|
|
NM_000488.4:c.885G=
MANE Select
|
NP_000479.1:p.Val295=
|
|
NM_001365052.2:c.741G=
|
NP_001351981.1:p.Val247=
|
|
NM_001386302.1:c.1008G=
|
NP_001373231.1:p.Val336=
|
|
NM_001386303.1:c.966G=
|
NP_001373232.1:p.Val322=
|
|
NM_001386304.1:c.864G=
|
NP_001373233.1:p.Val288=
|
|
NM_001386305.1:c.828G=
|
NP_001373234.1:p.Val276=
|
|
NM_001386306.1:c.669G=
|
NP_001373235.1:p.Val223=
|
|