ENST00000280362.8:c.302C>G
MANE Select
|
ENSP00000280362.3:p.Ala101Gly
|
|
ENST00000280362.7:c.302C>G
|
ENSP00000280362.3:p.Ala101Gly
|
|
ENST00000524931.1:c.98C>G
|
ENSP00000434688.1:p.Ala33Gly
|
|
ENST00000525803.1:c.*36C>G
|
ENSP00000431750.1:n.*36C>G
|
|
ENST00000527428.5:n.476C>G
|
|
|
ENST00000527635.1:n.343C>G
|
|
|
ENST00000528679.5:c.*111C>G
|
ENSP00000435895.1:n.*111C>G
|
|
ENST00000531175.1:n.253C>G
|
|
|
ENST00000531673.5:c.*111C>G
|
ENSP00000433469.1:n.*111C>G
|
|
NM_000317.2:c.302C>G
|
NP_000308.1:p.Ala101Gly
|
|
XM_011542943.1:c.263C>G
|
XP_011541245.1:p.Ala88Gly
|
|
NM_000317.3:c.302C>G
MANE Select
|
NP_000308.1:p.Ala101Gly
|
|