NM_000342.4:c.2317T=
MANE Select
|
NP_000333.1:p.Ser773=
|
ENST00000262418.12:c.2317T=
MANE Select
|
ENSP00000262418.6:p.Ser773=
|
NM_000342.3:c.2317T=
|
NP_000333.1:p.Ser773=
|
ENST00000262418.10:c.2317T=
|
ENSP00000262418.6:p.Ser773=
|
ENST00000399246.3:c.1219T=
|
ENSP00000382190.3:p.Ser407=
|
XM_005257593.3:c.2122T=
|
XP_005257650.1:p.Ser708=
|
XM_005257593.5:c.2122T=
|
XP_005257650.1:p.Ser708=
|
XM_011525129.1:c.2227T=
|
XP_011523431.1:p.Ser743=
|
XM_011525129.2:c.2227T=
|
XP_011523431.1:p.Ser743=
|
XM_011525130.1:c.*27T=
|
XP_011523432.1:n.*27T=
|