|
ENST00000367698.4:c.1296G=
MANE Select
|
ENSP00000356671.3:p.Val432=
|
|
|
ENST00000367698.3:c.1296G=
|
ENSP00000356671.3:p.Val432=
|
|
|
ENST00000617423.4:c.681G=
|
ENSP00000478688.1:p.Val227=
|
|
|
NM_000488.3:c.1296G= , LRG_577t1:c.1296G=
|
NP_000479.1:p.Val432=
|
|
|
XM_005245198.2:c.1152G=
|
XP_005245255.1:p.Val384=
|
|
|
NM_001365052.1:c.1152G=
|
NP_001351981.1:p.Val384=
|
|
|
NM_000488.4:c.1296G=
MANE Select
|
NP_000479.1:p.Val432=
|
|
|
NM_001365052.2:c.1152G=
|
NP_001351981.1:p.Val384=
|
|
|
NM_001386302.1:c.1419G=
|
NP_001373231.1:p.Val473=
|
|
|
NM_001386303.1:c.1377G=
|
NP_001373232.1:p.Val459=
|
|
|
NM_001386304.1:c.1275G=
|
NP_001373233.1:p.Val425=
|
|
|
NM_001386305.1:c.1239G=
|
NP_001373234.1:p.Val413=
|
|
|
NM_001386306.1:c.1080G=
|
NP_001373235.1:p.Val360=
|
|
