|
NM_021939.4:c.1613T>C
MANE Select
|
NP_068758.3:p.Met538Thr
|
|
ENST00000321562.9:c.1613T>C
MANE Select
|
ENSP00000317232.4:p.Met538Thr
|
|
NM_021939.3:c.1613T>C , LRG_12t1:c.1613T>C
|
NP_068758.3:p.Met538Thr
|
|
ENST00000321562.8:c.1613T>C
|
ENSP00000317232.4:p.Met538Thr
|
|
ENST00000455106.1:c.1024T>C
|
|
|
ENST00000464180.1:n.861T>C
|
|
|
ENST00000489591.5:c.*1397T>C
|
ENSP00000466352.1:n.*1397T>C
|
|
ENST00000490938.5:n.816T>C
|
|
|
ENST00000706683.1:c.1277T>C
|
ENSP00000516497.1:p.Met426Thr
|
|
XM_011525099.1:c.1670T>C
|
XP_011523401.1:p.Met557Thr
|
|
XM_011525099.3:c.1670T>C
|
XP_011523401.1:p.Met557Thr
|
|
XM_011525100.1:c.1397T>C
|
XP_011523402.1:p.Met466Thr
|
|
XM_011525100.2:c.1397T>C
|
XP_011523402.1:p.Met466Thr
|