ENST00000330684.4:c.4118A>T
MANE Select
|
ENSP00000332549.3:p.Asp1373Val
|
|
ENST00000535259.6:c.3304A>T
|
ENSP00000441572.3:p.Met1102Leu
|
|
ENST00000636273.2:n.3368A>T
|
|
|
ENST00000674742.1:c.3647A>T
|
ENSP00000502200.1:p.Asp1216Val
|
|
ENST00000675398.1:c.*1488A>T
|
ENSP00000502752.1:n.*1488A>T
|
|
ENST00000330684.3:c.4118A>T
|
ENSP00000332549.3:p.Asp1373Val
|
|
ENST00000396573.6:c.4118A>T
|
ENSP00000379818.2:p.Asp1373Val
|
|
ENST00000396575.6:c.3707A>T
|
ENSP00000379820.3:p.Asp1236Val
|
|
ENST00000461292.3:n.3414A>T
|
|
|
ENST00000535259.5:c.3364A>T
|
ENSP00000441572.2:p.Met1122Leu
|
|
ENST00000562109.5:c.3775A>T
|
ENSP00000454998.1:p.Met1259Leu
|
|
NM_000833.4:c.4118A>T
|
NP_000824.1:p.Asp1373Val
|
|
NM_001134407.2:c.4118A>T
|
NP_001127879.1:p.Asp1373Val
|
|
NM_001134408.2:c.3775A>T
|
NP_001127880.1:p.Met1259Leu
|
|
XM_011522456.1:c.3959A>T
|
XP_011520758.1:p.Asp1320Val
|
|
XM_011522457.1:c.3860A>T
|
XP_011520759.1:p.Asp1287Val
|
|
XM_011522458.1:c.3647A>T
|
XP_011520760.1:p.Asp1216Val
|
|
XM_011522459.1:c.3647A>T
|
XP_011520761.1:p.Asp1216Val
|
|
XM_011522460.1:c.3647A>T
|
XP_011520762.1:p.Asp1216Val
|
|
XM_011522461.1:c.3775A>T
|
XP_011520763.1:p.Met1259Leu
|
|
XM_011522458.3:c.3647A>T
|
XP_011520760.1:p.Asp1216Val
|
|
XM_011522461.3:c.3775A>T
|
XP_011520763.1:p.Met1259Leu
|
|
XM_017023172.1:c.4274A>T
|
XP_016878661.1:p.Asp1425Val
|
|
XM_017023173.1:c.3931A>T
|
XP_016878662.1:p.Met1311Leu
|
|
NM_001134407.3:c.4118A>T
MANE Select
|
NP_001127879.1:p.Asp1373Val
|
|
NM_000833.5:c.4118A>T
|
NP_000824.1:p.Asp1373Val
|
|