ENST00000344265.8:c.893T>G
|
ENSP00000342931.3:p.Val298Gly
|
|
ENST00000350375.7:c.815T>G
MANE Select
|
ENSP00000263781.2:p.Val272Gly
|
|
ENST00000344265.7:c.893T>G
|
ENSP00000342931.3:p.Val298Gly
|
|
ENST00000350375.6:c.815T>G
|
ENSP00000263781.2:p.Val272Gly
|
|
ENST00000560656.1:c.589T>G
|
ENSP00000452610.1:n.589T>G
|
|
ENST00000561167.5:c.590T>G
|
ENSP00000454072.1:p.Val197Gly
|
|
NM_000306.3:c.815T>G
|
NP_000297.1:p.Val272Gly
|
|
NM_001122757.2:c.893T>G
|
NP_001116229.1:p.Val298Gly
|
|
NM_000306.4:c.815T>G
MANE Select
|
NP_000297.1:p.Val272Gly
|
|
NM_001122757.3:c.893T>G
|
NP_001116229.1:p.Val298Gly
|
|