ENST00000280362.8:c.351C>T
MANE Select
|
ENSP00000280362.3:p.Asn117=
|
|
ENST00000280362.7:c.351C>T
|
ENSP00000280362.3:p.Asn117=
|
|
ENST00000524931.1:c.147C>T
|
ENSP00000434688.1:p.Asn49=
|
|
ENST00000525803.1:c.*85C>T
|
ENSP00000431750.1:n.*85C>T
|
|
ENST00000527428.5:n.488+235C>T
|
|
|
ENST00000527635.1:n.392C>T
|
|
|
ENST00000528679.5:c.*160C>T
|
ENSP00000435895.1:n.*160C>T
|
|
ENST00000531673.5:c.*123+235C>T
|
ENSP00000433469.1:n.*123+235C>T
|
|
NM_000317.2:c.351C>T
|
NP_000308.1:p.Asn117=
|
|
XM_011542943.1:c.312C>T
|
XP_011541245.1:p.Asn104=
|
|
NM_000317.3:c.351C>T
MANE Select
|
NP_000308.1:p.Asn117=
|
|