ENST00000330684.4:c.4142G>C
MANE Select
|
ENSP00000332549.3:p.Arg1381Thr
|
|
ENST00000535259.6:c.3328G>C
|
ENSP00000441572.3:p.Asp1110His
|
|
ENST00000636273.2:n.3392G>C
|
|
|
ENST00000674742.1:c.3671G>C
|
ENSP00000502200.1:p.Arg1224Thr
|
|
ENST00000675398.1:c.*1512G>C
|
ENSP00000502752.1:n.*1512G>C
|
|
ENST00000330684.3:c.4142G>C
|
ENSP00000332549.3:p.Arg1381Thr
|
|
ENST00000396573.6:c.4142G>C
|
ENSP00000379818.2:p.Arg1381Thr
|
|
ENST00000396575.6:c.3731G>C
|
ENSP00000379820.3:p.Arg1244Thr
|
|
ENST00000461292.3:n.3438G>C
|
|
|
ENST00000535259.5:c.3388G>C
|
ENSP00000441572.2:p.Asp1130His
|
|
ENST00000562109.5:c.3799G>C
|
ENSP00000454998.1:p.Asp1267His
|
|
NM_000833.4:c.4142G>C
|
NP_000824.1:p.Arg1381Thr
|
|
NM_001134407.2:c.4142G>C
|
NP_001127879.1:p.Arg1381Thr
|
|
NM_001134408.2:c.3799G>C
|
NP_001127880.1:p.Asp1267His
|
|
XM_011522456.1:c.3983G>C
|
XP_011520758.1:p.Arg1328Thr
|
|
XM_011522457.1:c.3884G>C
|
XP_011520759.1:p.Arg1295Thr
|
|
XM_011522458.1:c.3671G>C
|
XP_011520760.1:p.Arg1224Thr
|
|
XM_011522459.1:c.3671G>C
|
XP_011520761.1:p.Arg1224Thr
|
|
XM_011522460.1:c.3671G>C
|
XP_011520762.1:p.Arg1224Thr
|
|
XM_011522461.1:c.3799G>C
|
XP_011520763.1:p.Asp1267His
|
|
XM_011522458.3:c.3671G>C
|
XP_011520760.1:p.Arg1224Thr
|
|
XM_011522461.3:c.3799G>C
|
XP_011520763.1:p.Asp1267His
|
|
XM_017023172.1:c.4298G>C
|
XP_016878661.1:p.Arg1433Thr
|
|
XM_017023173.1:c.3955G>C
|
XP_016878662.1:p.Asp1319His
|
|
NM_001134407.3:c.4142G>C
MANE Select
|
NP_001127879.1:p.Arg1381Thr
|
|
NM_000833.5:c.4142G>C
|
NP_000824.1:p.Arg1381Thr
|
|