ENST00000403665.7:c.1219A=
MANE Select
|
ENSP00000384957.2:p.Thr407=
|
|
ENST00000264692.8:c.1057A=
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ENSP00000264692.5:p.Thr353=
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|
ENST00000403665.6:c.1219A=
|
ENSP00000384957.2:p.Thr407=
|
|
NM_000128.3:c.1219A= , LRG_583t1:c.1219A=
|
NP_000119.1:p.Thr407=
|
|
XM_005262821.2:c.1222A=
|
XP_005262878.1:p.Thr408=
|
|
XM_005262822.2:c.1222A=
|
XP_005262879.1:p.Thr408=
|
|
XM_005262823.2:c.952A=
|
XP_005262880.1:p.Thr318=
|
|
XM_005262824.1:c.1222A=
|
XP_005262881.1:p.Thr408=
|
|
XM_006714137.1:c.1174A=
|
XP_006714200.1:p.Thr392=
|
|
XR_938706.1:n.1627A=
|
|
|
XR_938707.1:n.1627A=
|
|
|
XM_005262821.4:c.1222A=
|
XP_005262878.1:p.Thr408=
|
|
XM_005262822.4:c.1222A=
|
XP_005262879.1:p.Thr408=
|
|
XM_005262823.4:c.952A=
|
XP_005262880.1:p.Thr318=
|
|
XM_006714137.3:c.1174A=
|
XP_006714200.1:p.Thr392=
|
|
XM_017007884.2:c.*2191A=
|
XP_016863373.1:n.*2191A=
|
|
XR_001741172.2:n.1693A=
|
|
|
NM_000128.4:c.1219A=
MANE Select
|
NP_000119.1:p.Thr407=
|
|