ENST00000367698.4:c.1343C>A
MANE Select
|
ENSP00000356671.3:p.Pro448His
|
|
ENST00000367698.3:c.1343C>A
|
ENSP00000356671.3:p.Pro448His
|
|
ENST00000617423.4:c.728C>A
|
ENSP00000478688.1:p.Pro243His
|
|
NM_000488.3:c.1343C>A , LRG_577t1:c.1343C>A
|
NP_000479.1:p.Pro448His
|
|
XM_005245198.2:c.1199C>A
|
XP_005245255.1:p.Pro400His
|
|
NM_001365052.1:c.1199C>A
|
NP_001351981.1:p.Pro400His
|
|
NM_000488.4:c.1343C>A
MANE Select
|
NP_000479.1:p.Pro448His
|
|
NM_001365052.2:c.1199C>A
|
NP_001351981.1:p.Pro400His
|
|
NM_001386302.1:c.1466C>A
|
NP_001373231.1:p.Pro489His
|
|
NM_001386303.1:c.1424C>A
|
NP_001373232.1:p.Pro475His
|
|
NM_001386304.1:c.1322C>A
|
NP_001373233.1:p.Pro441His
|
|
NM_001386305.1:c.1286C>A
|
NP_001373234.1:p.Pro429His
|
|
NM_001386306.1:c.1127C>A
|
NP_001373235.1:p.Pro376His
|
|