ENST00000263341.7:c.312C>T
MANE Select
|
ENSP00000263341.2:p.Phe104=
|
|
ENST00000263341.6:c.312C>T
|
ENSP00000263341.2:p.Phe104=
|
|
ENST00000416750.1:c.312C>T
|
ENSP00000400854.1:p.Phe104=
|
|
ENST00000418817.5:c.312C>T
|
ENSP00000407219.1:p.Phe104=
|
|
ENST00000432018.5:c.312C>T
|
ENSP00000409680.1:p.Phe104=
|
|
ENST00000487639.1:n.213C>T
|
|
|
ENST00000491056.5:n.1119C>T
|
|
|
NM_000576.2:c.312C>T
|
NP_000567.1:p.Phe104=
|
|
XM_006712496.1:c.78C>T
|
XP_006712559.1:p.Phe26=
|
|
XM_017003988.2:c.219C>T
|
XP_016859477.1:p.Phe73=
|
|
NM_000576.3:c.312C>T
MANE Select
|
NP_000567.1:p.Phe104=
|
|