|
ENST00000338468.8:c.1170G>T
|
ENSP00000343589.4:n.1170G>T
|
|
|
ENST00000366894.6:c.1051G>T
|
ENSP00000355860.2:n.1051G>T
|
|
|
ENST00000366898.6:c.1292G>T
MANE Select
|
ENSP00000355865.1:p.Cys431Phe
|
|
|
ENST00000673871.1:c.1373G>T
|
|
|
|
ENST00000674006.1:n.677G>T
|
|
|
|
ENST00000674436.1:n.928G>T
|
|
|
|
ENST00000338468.7:c.719G>T
|
ENSP00000343589.3:p.Cys240Phe
|
|
|
ENST00000366894.5:c.719G>T
|
ENSP00000355860.1:p.Cys240Phe
|
|
|
ENST00000366896.5:c.845G>T
|
ENSP00000355862.1:p.Cys282Phe
|
|
|
ENST00000366897.5:c.1208G>T
|
ENSP00000355863.1:p.Cys403Phe
|
|
|
ENST00000366898.5:c.1292G>T
|
ENSP00000355865.1:p.Cys431Phe
|
|
|
ENST00000479615.5:c.*68G>T
|
ENSP00000434414.1:n.*68G>T
|
|
|
ENST00000610470.4:c.425G>T
|
ENSP00000483773.1:p.Cys142Phe
|
|
|
NM_004562.2:c.1292G>T
|
NP_004553.2:p.Cys431Phe
|
|
|
NM_013987.2:c.1208G>T
|
NP_054642.2:p.Cys403Phe
|
|
|
NM_013988.2:c.845G>T
|
NP_054643.2:p.Cys282Phe
|
|
|
XM_011535863.1:c.1289G>T
|
XP_011534165.1:p.Cys430Phe
|
|
|
XM_017010908.1:c.1406G>T
|
XP_016866397.1:p.Cys469Phe
|
|
|
XM_017010909.2:c.1052G>T
|
XP_016866398.1:p.Cys351Phe
|
|
|
XM_024446449.1:c.1055G>T
|
XP_024302217.1:p.Cys352Phe
|
|
|
XR_001743443.2:n.1484G>T
|
|
|
|
NM_004562.3:c.1292G>T
MANE Select
|
NP_004553.2:p.Cys431Phe
|
|
|
NM_013987.3:c.1208G>T
|
NP_054642.2:p.Cys403Phe
|
|
|
NM_013988.3:c.845G>T
|
NP_054643.2:p.Cys282Phe
|
|
