ENST00000399391.7:c.462G>C
|
ENSP00000382323.2:p.Ala154=
|
|
ENST00000399397.6:c.426G>C
MANE Select
|
ENSP00000382329.2:p.Ala142=
|
|
ENST00000399391.6:c.462G>C
|
ENSP00000382323.2:p.Ala154=
|
|
ENST00000399397.5:c.426G>C
|
ENSP00000382329.2:p.Ala142=
|
|
ENST00000428619.1:c.243G>C
|
ENSP00000399057.2:p.Ala81=
|
|
ENST00000498332.5:n.332G>C
|
|
|
NM_001277269.1:c.462G>C
|
NP_001264198.1:p.Ala154=
|
|
NM_001292063.1:c.426G>C
|
NP_001278992.1:p.Ala142=
|
|
NM_001277269.2:c.462G>C
|
NP_001264198.1:p.Ala154=
|
|
NM_001292063.2:c.426G>C
MANE Select
|
NP_001278992.1:p.Ala142=
|
|