ENST00000403665.7:c.1186C>A
MANE Select
|
ENSP00000384957.2:p.Arg396Ser
|
|
ENST00000264692.8:c.1024C>A
|
ENSP00000264692.5:p.Arg342Ser
|
|
ENST00000403665.6:c.1186C>A
|
ENSP00000384957.2:p.Arg396Ser
|
|
NM_000128.3:c.1186C>A , LRG_583t1:c.1186C>A
|
NP_000119.1:p.Arg396Ser
|
|
XM_005262821.2:c.1189C>A
|
XP_005262878.1:p.Arg397Ser
|
|
XM_005262822.2:c.1189C>A
|
XP_005262879.1:p.Arg397Ser
|
|
XM_005262823.2:c.919C>A
|
XP_005262880.1:p.Arg307Ser
|
|
XM_005262824.1:c.1189C>A
|
XP_005262881.1:p.Arg397Ser
|
|
XM_006714137.1:c.1141C>A
|
XP_006714200.1:p.Arg381Ser
|
|
XR_938706.1:n.1594C>A
|
|
|
XR_938707.1:n.1594C>A
|
|
|
XM_005262821.4:c.1189C>A
|
XP_005262878.1:p.Arg397Ser
|
|
XM_005262822.4:c.1189C>A
|
XP_005262879.1:p.Arg397Ser
|
|
XM_005262823.4:c.919C>A
|
XP_005262880.1:p.Arg307Ser
|
|
XM_006714137.3:c.1141C>A
|
XP_006714200.1:p.Arg381Ser
|
|
XM_017007884.2:c.*2158C>A
|
XP_016863373.1:n.*2158C>A
|
|
XM_017007885.2:c.*54C>A
|
XP_016863374.1:n.*54C>A
|
|
XR_001741172.2:n.1660C>A
|
|
|
NM_000128.4:c.1186C>A
MANE Select
|
NP_000119.1:p.Arg396Ser
|
|