ENST00000338468.8:c.1230G>C
|
ENSP00000343589.4:n.1230G>C
|
|
ENST00000366894.6:c.1111G>C
|
ENSP00000355860.2:n.1111G>C
|
|
ENST00000366898.6:c.1352G>C
MANE Select
|
ENSP00000355865.1:p.Cys451Ser
|
|
ENST00000673871.1:c.1433G>C
|
|
|
ENST00000674006.1:n.737G>C
|
|
|
ENST00000674436.1:n.988G>C
|
|
|
ENST00000338468.7:c.779G>C
|
ENSP00000343589.3:p.Cys260Ser
|
|
ENST00000366894.5:c.779G>C
|
ENSP00000355860.1:p.Cys260Ser
|
|
ENST00000366896.5:c.905G>C
|
ENSP00000355862.1:p.Cys302Ser
|
|
ENST00000366897.5:c.1268G>C
|
ENSP00000355863.1:p.Cys423Ser
|
|
ENST00000366898.5:c.1352G>C
|
ENSP00000355865.1:p.Cys451Ser
|
|
ENST00000479615.5:c.*128G>C
|
ENSP00000434414.1:n.*128G>C
|
|
ENST00000610470.4:c.485G>C
|
ENSP00000483773.1:p.Cys162Ser
|
|
NM_004562.2:c.1352G>C
|
NP_004553.2:p.Cys451Ser
|
|
NM_013987.2:c.1268G>C
|
NP_054642.2:p.Cys423Ser
|
|
NM_013988.2:c.905G>C
|
NP_054643.2:p.Cys302Ser
|
|
XM_011535863.1:c.1349G>C
|
XP_011534165.1:p.Cys450Ser
|
|
XM_017010908.1:c.1466G>C
|
XP_016866397.1:p.Cys489Ser
|
|
XM_017010909.2:c.1112G>C
|
XP_016866398.1:p.Cys371Ser
|
|
XM_024446449.1:c.1115G>C
|
XP_024302217.1:p.Cys372Ser
|
|
XR_001743443.2:n.1544G>C
|
|
|
NM_004562.3:c.1352G>C
MANE Select
|
NP_004553.2:p.Cys451Ser
|
|
NM_013987.3:c.1268G>C
|
NP_054642.2:p.Cys423Ser
|
|
NM_013988.3:c.905G>C
|
NP_054643.2:p.Cys302Ser
|
|