ENST00000403665.7:c.1126A>G
MANE Select
|
ENSP00000384957.2:p.Met376Val
|
|
ENST00000264692.8:c.964A>G
|
ENSP00000264692.5:p.Met322Val
|
|
ENST00000403665.6:c.1126A>G
|
ENSP00000384957.2:p.Met376Val
|
|
ENST00000452239.1:c.573A>G
|
|
|
NM_000128.3:c.1126A>G , LRG_583t1:c.1126A>G
|
NP_000119.1:p.Met376Val
|
|
XM_005262821.2:c.1129A>G
|
XP_005262878.1:p.Met377Val
|
|
XM_005262822.2:c.1129A>G
|
XP_005262879.1:p.Met377Val
|
|
XM_005262823.2:c.859A>G
|
XP_005262880.1:p.Met287Val
|
|
XM_005262824.1:c.1129A>G
|
XP_005262881.1:p.Met377Val
|
|
XM_006714137.1:c.1081A>G
|
XP_006714200.1:p.Met361Val
|
|
XR_938706.1:n.1481A>G
|
|
|
XR_938707.1:n.1481A>G
|
|
|
XM_005262821.4:c.1129A>G
|
XP_005262878.1:p.Met377Val
|
|
XM_005262822.4:c.1129A>G
|
XP_005262879.1:p.Met377Val
|
|
XM_005262823.4:c.859A>G
|
XP_005262880.1:p.Met287Val
|
|
XM_006714137.3:c.1081A>G
|
XP_006714200.1:p.Met361Val
|
|
XM_017007884.2:c.1129A>G
|
XP_016863373.1:p.Met377Val
|
|
XM_017007885.2:c.1129A>G
|
XP_016863374.1:p.Met377Val
|
|
XM_017007886.2:c.1126A>G
|
XP_016863375.1:p.Met376Val
|
|
XR_001741172.2:n.1547A>G
|
|
|
NM_000128.4:c.1126A>G
MANE Select
|
NP_000119.1:p.Met376Val
|
|