ENST00000344265.8:c.544G>T
|
ENSP00000342931.3:p.Ala182Ser
|
|
ENST00000350375.7:c.466G>T
MANE Select
|
ENSP00000263781.2:p.Ala156Ser
|
|
ENST00000344265.7:c.544G>T
|
ENSP00000342931.3:p.Ala182Ser
|
|
ENST00000350375.6:c.466G>T
|
ENSP00000263781.2:p.Ala156Ser
|
|
ENST00000560656.1:c.439+2079G>T
|
ENSP00000452610.1:n.439+2079G>T
|
|
ENST00000561167.5:c.241G>T
|
ENSP00000454072.1:p.Ala81Ser
|
|
NM_000306.3:c.466G>T
|
NP_000297.1:p.Ala156Ser
|
|
NM_001122757.2:c.544G>T
|
NP_001116229.1:p.Ala182Ser
|
|
NM_000306.4:c.466G>T
MANE Select
|
NP_000297.1:p.Ala156Ser
|
|
NM_001122757.3:c.544G>T
|
NP_001116229.1:p.Ala182Ser
|
|