ENST00000344265.8:c.413G>T
|
ENSP00000342931.3:p.Arg138Met
|
|
ENST00000350375.7:c.335G>T
MANE Select
|
ENSP00000263781.2:p.Arg112Met
|
|
ENST00000344265.7:c.413G>T
|
ENSP00000342931.3:p.Arg138Met
|
|
ENST00000350375.6:c.335G>T
|
ENSP00000263781.2:p.Arg112Met
|
|
ENST00000560656.1:c.335G>T
|
ENSP00000452610.1:p.Arg112Met
|
|
ENST00000561167.5:c.215-2157G>T
|
ENSP00000454072.1:n.215-2157G>T
|
|
NM_000306.3:c.335G>T
|
NP_000297.1:p.Arg112Met
|
|
NM_001122757.2:c.413G>T
|
NP_001116229.1:p.Arg138Met
|
|
NM_000306.4:c.335G>T
MANE Select
|
NP_000297.1:p.Arg112Met
|
|
NM_001122757.3:c.413G>T
|
NP_001116229.1:p.Arg138Met
|
|