ENST00000576204.6:n.883C>A
|
|
|
ENST00000622290.5:c.*192C>A
|
ENSP00000483331.2:n.*192C>A
|
|
ENST00000205557.12:c.4020C>A
MANE Select
|
ENSP00000205557.7:p.Ser1340=
|
|
ENST00000640696.1:c.834C>A
|
ENSP00000492197.1:p.Ser278=
|
|
ENST00000205557.11:c.4020C>A
|
ENSP00000205557.7:p.Ser1340=
|
|
ENST00000456970.6:c.3645C>A
|
ENSP00000405002.2:n.3645C>A
|
|
ENST00000576204.5:n.883C>A
|
|
|
ENST00000622290.4:c.*1229C>A
|
ENSP00000483331.1:n.*1229C>A
|
|
NM_001171.5:c.4020C>A
|
NP_001162.4:p.Ser1340=
|
|
XM_011522479.1:c.3987C>A
|
XP_011520781.1:p.Ser1329=
|
|
XM_011522480.1:c.3678C>A
|
XP_011520782.1:p.Ser1226=
|
|
XM_011522481.1:c.3678C>A
|
XP_011520783.1:p.Ser1226=
|
|
XR_933134.1:n.539-4887G>T
|
|
|
NM_001351800.1:c.3678C>A
|
NP_001338729.1:p.Ser1226=
|
|
NR_147784.1:n.3682C>A
|
|
|
XM_011522479.2:c.3987C>A
|
XP_011520781.1:p.Ser1329=
|
|
XM_011522481.3:c.3678C>A
|
XP_011520783.1:p.Ser1226=
|
|
XM_017023212.1:c.3852C>A
|
XP_016878701.1:p.Ser1284=
|
|
XM_024450261.1:c.4056C>A
|
XP_024306029.1:p.Ser1352=
|
|
NM_001171.6:c.4020C>A
MANE Select
|
NP_001162.5:p.Ser1340=
|
|