ENST00000367698.4:c.1133C>A
MANE Select
|
ENSP00000356671.3:p.Pro378His
|
|
ENST00000367698.3:c.1133C>A
|
ENSP00000356671.3:p.Pro378His
|
|
ENST00000617423.4:c.560-2079C>A
|
ENSP00000478688.1:n.560-2079C>A
|
|
NM_000488.3:c.1133C>A , LRG_577t1:c.1133C>A
|
NP_000479.1:p.Pro378His
|
|
XM_005245198.2:c.989C>A
|
XP_005245255.1:p.Pro330His
|
|
NM_001365052.1:c.989C>A
|
NP_001351981.1:p.Pro330His
|
|
NM_000488.4:c.1133C>A
MANE Select
|
NP_000479.1:p.Pro378His
|
|
NM_001365052.2:c.989C>A
|
NP_001351981.1:p.Pro330His
|
|
NM_001386302.1:c.1256C>A
|
NP_001373231.1:p.Pro419His
|
|
NM_001386303.1:c.1214C>A
|
NP_001373232.1:p.Pro405His
|
|
NM_001386304.1:c.1112C>A
|
NP_001373233.1:p.Pro371His
|
|
NM_001386305.1:c.1076C>A
|
NP_001373234.1:p.Pro359His
|
|
NM_001386306.1:c.917C>A
|
NP_001373235.1:p.Pro306His
|
|