ENST00000403665.7:c.1223C=
MANE Select
|
ENSP00000384957.2:p.Thr408=
|
|
ENST00000264692.8:c.1061C=
|
ENSP00000264692.5:p.Thr354=
|
|
ENST00000403665.6:c.1223C=
|
ENSP00000384957.2:p.Thr408=
|
|
NM_000128.3:c.1223C= , LRG_583t1:c.1223C=
|
NP_000119.1:p.Thr408=
|
|
XM_005262821.2:c.1226C=
|
XP_005262878.1:p.Thr409=
|
|
XM_005262822.2:c.1226C=
|
XP_005262879.1:p.Thr409=
|
|
XM_005262823.2:c.956C=
|
XP_005262880.1:p.Thr319=
|
|
XM_005262824.1:c.1226C=
|
XP_005262881.1:p.Thr409=
|
|
XM_006714137.1:c.1178C=
|
XP_006714200.1:p.Thr393=
|
|
XR_938706.1:n.1631C=
|
|
|
XR_938707.1:n.1631C=
|
|
|
XM_005262821.4:c.1226C=
|
XP_005262878.1:p.Thr409=
|
|
XM_005262822.4:c.1226C=
|
XP_005262879.1:p.Thr409=
|
|
XM_005262823.4:c.956C=
|
XP_005262880.1:p.Thr319=
|
|
XM_006714137.3:c.1178C=
|
XP_006714200.1:p.Thr393=
|
|
XM_017007884.2:c.*2195C=
|
XP_016863373.1:n.*2195C=
|
|
XR_001741172.2:n.1697C=
|
|
|
NM_000128.4:c.1223C=
MANE Select
|
NP_000119.1:p.Thr408=
|
|