ENST00000403665.7:c.1188T>C
MANE Select
|
ENSP00000384957.2:p.Arg396=
|
|
ENST00000264692.8:c.1026T>C
|
ENSP00000264692.5:p.Arg342=
|
|
ENST00000403665.6:c.1188T>C
|
ENSP00000384957.2:p.Arg396=
|
|
NM_000128.3:c.1188T>C , LRG_583t1:c.1188T>C
|
NP_000119.1:p.Arg396=
|
|
XM_005262821.2:c.1191T>C
|
XP_005262878.1:p.Arg397=
|
|
XM_005262822.2:c.1191T>C
|
XP_005262879.1:p.Arg397=
|
|
XM_005262823.2:c.921T>C
|
XP_005262880.1:p.Arg307=
|
|
XM_005262824.1:c.1191T>C
|
XP_005262881.1:p.Arg397=
|
|
XM_006714137.1:c.1143T>C
|
XP_006714200.1:p.Arg381=
|
|
XR_938706.1:n.1596T>C
|
|
|
XR_938707.1:n.1596T>C
|
|
|
XM_005262821.4:c.1191T>C
|
XP_005262878.1:p.Arg397=
|
|
XM_005262822.4:c.1191T>C
|
XP_005262879.1:p.Arg397=
|
|
XM_005262823.4:c.921T>C
|
XP_005262880.1:p.Arg307=
|
|
XM_006714137.3:c.1143T>C
|
XP_006714200.1:p.Arg381=
|
|
XM_017007884.2:c.*2160T>C
|
XP_016863373.1:n.*2160T>C
|
|
XM_017007885.2:c.*56T>C
|
XP_016863374.1:n.*56T>C
|
|
XR_001741172.2:n.1662T>C
|
|
|
NM_000128.4:c.1188T>C
MANE Select
|
NP_000119.1:p.Arg396=
|
|