ENST00000403665.7:c.1069A>T
MANE Select
|
ENSP00000384957.2:p.Thr357Ser
|
|
ENST00000264692.8:c.907A>T
|
ENSP00000264692.5:p.Thr303Ser
|
|
ENST00000403665.6:c.1069A>T
|
ENSP00000384957.2:p.Thr357Ser
|
|
ENST00000452239.1:c.516A>T
|
|
|
NM_000128.3:c.1069A>T , LRG_583t1:c.1069A>T
|
NP_000119.1:p.Thr357Ser
|
|
XM_005262821.2:c.1072A>T
|
XP_005262878.1:p.Thr358Ser
|
|
XM_005262822.2:c.1072A>T
|
XP_005262879.1:p.Thr358Ser
|
|
XM_005262823.2:c.802A>T
|
XP_005262880.1:p.Thr268Ser
|
|
XM_005262824.1:c.1072A>T
|
XP_005262881.1:p.Thr358Ser
|
|
XM_006714137.1:c.1024A>T
|
XP_006714200.1:p.Thr342Ser
|
|
XR_938706.1:n.1424A>T
|
|
|
XR_938707.1:n.1424A>T
|
|
|
XM_005262821.4:c.1072A>T
|
XP_005262878.1:p.Thr358Ser
|
|
XM_005262822.4:c.1072A>T
|
XP_005262879.1:p.Thr358Ser
|
|
XM_005262823.4:c.802A>T
|
XP_005262880.1:p.Thr268Ser
|
|
XM_006714137.3:c.1024A>T
|
XP_006714200.1:p.Thr342Ser
|
|
XM_017007884.2:c.1072A>T
|
XP_016863373.1:p.Thr358Ser
|
|
XM_017007885.2:c.1072A>T
|
XP_016863374.1:p.Thr358Ser
|
|
XM_017007886.2:c.1069A>T
|
XP_016863375.1:p.Thr357Ser
|
|
XR_001741172.2:n.1490A>T
|
|
|
NM_000128.4:c.1069A>T
MANE Select
|
NP_000119.1:p.Thr357Ser
|
|