|
ENST00000367698.4:c.959C>A
MANE Select
|
ENSP00000356671.3:p.Pro320His
|
|
|
ENST00000367698.3:c.959C>A
|
ENSP00000356671.3:p.Pro320His
|
|
|
ENST00000487183.1:n.610C>A
|
|
|
|
ENST00000617423.4:c.559+2118C>A
|
ENSP00000478688.1:n.559+2118C>A
|
|
|
NM_000488.3:c.959C>A , LRG_577t1:c.959C>A
|
NP_000479.1:p.Pro320His
|
|
|
XM_005245198.2:c.815C>A
|
XP_005245255.1:p.Pro272His
|
|
|
NM_001365052.1:c.815C>A
|
NP_001351981.1:p.Pro272His
|
|
|
NM_000488.4:c.959C>A
MANE Select
|
NP_000479.1:p.Pro320His
|
|
|
NM_001365052.2:c.815C>A
|
NP_001351981.1:p.Pro272His
|
|
|
NM_001386302.1:c.1082C>A
|
NP_001373231.1:p.Pro361His
|
|
|
NM_001386303.1:c.1040C>A
|
NP_001373232.1:p.Pro347His
|
|
|
NM_001386304.1:c.938C>A
|
NP_001373233.1:p.Pro313His
|
|
|
NM_001386305.1:c.902C>A
|
NP_001373234.1:p.Pro301His
|
|
|
NM_001386306.1:c.743C>A
|
NP_001373235.1:p.Pro248His
|
|
