ENST00000367698.4:c.960T=
MANE Select
|
ENSP00000356671.3:p.Pro320=
|
|
ENST00000367698.3:c.960T=
|
ENSP00000356671.3:p.Pro320=
|
|
ENST00000487183.1:n.611T=
|
|
|
ENST00000617423.4:c.559+2119T=
|
ENSP00000478688.1:n.559+2119T=
|
|
NM_000488.3:c.960T= , LRG_577t1:c.960T=
|
NP_000479.1:p.Pro320=
|
|
XM_005245198.2:c.816T=
|
XP_005245255.1:p.Pro272=
|
|
NM_001365052.1:c.816T=
|
NP_001351981.1:p.Pro272=
|
|
NM_000488.4:c.960T=
MANE Select
|
NP_000479.1:p.Pro320=
|
|
NM_001365052.2:c.816T=
|
NP_001351981.1:p.Pro272=
|
|
NM_001386302.1:c.1083T=
|
NP_001373231.1:p.Pro361=
|
|
NM_001386303.1:c.1041T=
|
NP_001373232.1:p.Pro347=
|
|
NM_001386304.1:c.939T=
|
NP_001373233.1:p.Pro313=
|
|
NM_001386305.1:c.903T=
|
NP_001373234.1:p.Pro301=
|
|
NM_001386306.1:c.744T=
|
NP_001373235.1:p.Pro248=
|
|