ENST00000333360.12:c.426C=
(SELE)
MANE Select
|
ENSP00000331736.7:p.Ala142=
|
|
ENST00000333360.11:c.426C=
(SELE)
|
ENSP00000331736.7:p.Ala142=
|
|
ENST00000367774.1:c.426C=
(SELE)
|
ENSP00000356748.1:p.Ala142=
|
|
ENST00000367775.5:c.426C=
(SELE)
|
ENSP00000356749.1:p.Ala142=
|
|
ENST00000367776.5:c.426C=
(SELE)
|
ENSP00000356750.1:p.Ala142=
|
|
ENST00000367777.5:c.426C=
(SELE)
|
ENSP00000356751.1:p.Ala142=
|
|
ENST00000461085.1:n.109C=
(SELE)
|
|
|
ENST00000498289.5:n.851+48006G=
(FIRRM)
|
|
|
NM_000450.2:c.426C=
(SELE)
MANE Select
|
NP_000441.2:p.Ala142=
|
|