ENST00000682422.1:n.742C>G
|
|
|
ENST00000682545.1:c.*167C>G
|
ENSP00000508402.1:n.*167C>G
|
|
ENST00000682887.1:c.1562C>G
|
ENSP00000506946.1:n.1562C>G
|
|
ENST00000683302.1:c.1092C>G
|
ENSP00000507885.1:p.Thr364=
|
|
ENST00000683557.1:c.752C>G
|
ENSP00000508029.1:p.Pro251Arg
|
|
ENST00000367282.6:c.1161C>G
MANE Select
|
ENSP00000356251.4:p.Thr387=
|
|
ENST00000367282.5:c.1161C>G
|
ENSP00000356251.4:p.Thr387=
|
|
NM_004767.3:c.1161C>G
|
NP_004758.3:p.Thr387=
|
|
XM_011510158.1:c.600C>G
|
XP_011508460.1:p.Thr200=
|
|
NM_004767.4:c.1161C>G
|
NP_004758.3:p.Thr387=
|
|
XM_011510158.2:c.600C>G
|
XP_011508460.1:p.Thr200=
|
|
NM_004767.5:c.1161C>G
MANE Select
|
NP_004758.3:p.Thr387=
|
|