ENST00000367698.4:c.1059C=
MANE Select
|
ENSP00000356671.3:p.Pro353=
|
|
ENST00000367698.3:c.1059C=
|
ENSP00000356671.3:p.Pro353=
|
|
ENST00000617423.4:c.560-2153C=
|
ENSP00000478688.1:n.560-2153C=
|
|
NM_000488.3:c.1059C= , LRG_577t1:c.1059C=
|
NP_000479.1:p.Pro353=
|
|
XM_005245198.2:c.915C=
|
XP_005245255.1:p.Pro305=
|
|
NM_001365052.1:c.915C=
|
NP_001351981.1:p.Pro305=
|
|
NM_000488.4:c.1059C=
MANE Select
|
NP_000479.1:p.Pro353=
|
|
NM_001365052.2:c.915C=
|
NP_001351981.1:p.Pro305=
|
|
NM_001386302.1:c.1182C=
|
NP_001373231.1:p.Pro394=
|
|
NM_001386303.1:c.1140C=
|
NP_001373232.1:p.Pro380=
|
|
NM_001386304.1:c.1038C=
|
NP_001373233.1:p.Pro346=
|
|
NM_001386305.1:c.1002C=
|
NP_001373234.1:p.Pro334=
|
|
NM_001386306.1:c.843C=
|
NP_001373235.1:p.Pro281=
|
|