|
NM_002834.5:c.1658C>T
MANE Select
|
NP_002825.3:p.Thr553Met
|
|
ENST00000351677.7:c.1658C>T
MANE Select
|
ENSP00000340944.3:p.Thr553Met
|
|
NM_001330437.1:c.1670C>T
|
NP_001317366.1:p.Thr557Met
|
|
NM_001330437.2:c.1670C>T
|
NP_001317366.1:p.Thr557Met
|
|
NM_001374625.1:c.1655C>T
|
NP_001361554.1:p.Thr552Met
|
|
NM_002834.3:c.1658C>T , LRG_614t1:c.1658C>T
|
NP_002825.3:p.Thr553Met
|
|
NM_002834.4:c.1658C>T
|
NP_002825.3:p.Thr553Met
|
|
ENST00000351677.6:c.1658C>T
|
ENSP00000340944.2:p.Thr553Met
|
|
ENST00000635625.1:c.1670C>T
|
ENSP00000489597.1:p.Thr557Met
|
|
ENST00000639857.2:c.1658C>T
|
ENSP00000491593.2:p.Thr553Met
|
|
ENST00000685487.1:c.*860C>T
|
ENSP00000508503.1:n.*860C>T
|
|
ENST00000687120.1:n.1041C>T
|
|
|
ENST00000687906.1:c.1544C>T
|
ENSP00000509536.1:p.Thr515Met
|
|
ENST00000688597.1:c.1283C>T
|
ENSP00000510628.1:p.Thr428Met
|
|
ENST00000688701.1:n.902C>T
|
|
|
ENST00000690210.1:c.1658C>T
|
ENSP00000509272.1:p.Thr553Met
|
|
ENST00000690472.1:n.867C>T
|
|
|
ENST00000692624.1:c.*204C>T
|
ENSP00000508953.1:n.*204C>T
|
|
XM_006719526.1:c.1670C>T
|
XP_006719589.1:p.Thr557Met
|
|
XM_006719527.1:c.1556C>T
|
XP_006719590.1:p.Thr519Met
|
|
XM_011538613.1:c.1667C>T
|
XP_011536915.1:p.Thr556Met
|
|
XM_011538613.2:c.1667C>T
|
XP_011536915.1:p.Thr556Met
|
|
XM_017019722.1:c.1655C>T
|
XP_016875211.1:p.Thr552Met
|
