ENST00000367698.4:c.1096C>T
MANE Select
|
ENSP00000356671.3:p.Gln366Ter
|
|
ENST00000367698.3:c.1096C>T
|
ENSP00000356671.3:p.Gln366Ter
|
|
ENST00000617423.4:c.560-2116C>T
|
ENSP00000478688.1:n.560-2116C>T
|
|
NM_000488.3:c.1096C>T , LRG_577t1:c.1096C>T
|
NP_000479.1:p.Gln366Ter
|
|
XM_005245198.2:c.952C>T
|
XP_005245255.1:p.Gln318Ter
|
|
NM_001365052.1:c.952C>T
|
NP_001351981.1:p.Gln318Ter
|
|
NM_000488.4:c.1096C>T
MANE Select
|
NP_000479.1:p.Gln366Ter
|
|
NM_001365052.2:c.952C>T
|
NP_001351981.1:p.Gln318Ter
|
|
NM_001386302.1:c.1219C>T
|
NP_001373231.1:p.Gln407Ter
|
|
NM_001386303.1:c.1177C>T
|
NP_001373232.1:p.Gln393Ter
|
|
NM_001386304.1:c.1075C>T
|
NP_001373233.1:p.Gln359Ter
|
|
NM_001386305.1:c.1039C>T
|
NP_001373234.1:p.Gln347Ter
|
|
NM_001386306.1:c.880C>T
|
NP_001373235.1:p.Gln294Ter
|
|