ENST00000367698.4:c.914C>A
MANE Select
|
ENSP00000356671.3:p.Pro305His
|
|
ENST00000367698.3:c.914C>A
|
ENSP00000356671.3:p.Pro305His
|
|
ENST00000487183.1:n.565C>A
|
|
|
ENST00000617423.4:c.559+2073C>A
|
ENSP00000478688.1:n.559+2073C>A
|
|
NM_000488.3:c.914C>A , LRG_577t1:c.914C>A
|
NP_000479.1:p.Pro305His
|
|
XM_005245198.2:c.770C>A
|
XP_005245255.1:p.Pro257His
|
|
NM_001365052.1:c.770C>A
|
NP_001351981.1:p.Pro257His
|
|
NM_000488.4:c.914C>A
MANE Select
|
NP_000479.1:p.Pro305His
|
|
NM_001365052.2:c.770C>A
|
NP_001351981.1:p.Pro257His
|
|
NM_001386302.1:c.1037C>A
|
NP_001373231.1:p.Pro346His
|
|
NM_001386303.1:c.995C>A
|
NP_001373232.1:p.Pro332His
|
|
NM_001386304.1:c.893C>A
|
NP_001373233.1:p.Pro298His
|
|
NM_001386305.1:c.857C>A
|
NP_001373234.1:p.Pro286His
|
|
NM_001386306.1:c.698C>A
|
NP_001373235.1:p.Pro233His
|
|