ENST00000330684.4:c.3962A=
MANE Select
|
ENSP00000332549.3:p.Glu1321=
|
|
ENST00000535259.6:c.3302-154A=
|
ENSP00000441572.3:n.3302-154A=
|
|
ENST00000636273.2:n.3366-154A=
|
|
|
ENST00000674742.1:c.3491A=
|
ENSP00000502200.1:p.Glu1164=
|
|
ENST00000675398.1:c.*1332A=
|
ENSP00000502752.1:n.*1332A=
|
|
ENST00000330684.3:c.3962A=
|
ENSP00000332549.3:p.Glu1321=
|
|
ENST00000396573.6:c.3962A=
|
ENSP00000379818.2:p.Glu1321=
|
|
ENST00000396575.6:c.3551A=
|
ENSP00000379820.3:p.Glu1184=
|
|
ENST00000461292.3:n.3412-154A=
|
|
|
ENST00000535259.5:c.3362-154A=
|
ENSP00000441572.2:n.3362-154A=
|
|
ENST00000562109.5:c.3773-154A=
|
ENSP00000454998.1:n.3773-154A=
|
|
NM_000833.4:c.3962A=
|
NP_000824.1:p.Glu1321=
|
|
NM_001134407.2:c.3962A=
|
NP_001127879.1:p.Glu1321=
|
|
NM_001134408.2:c.3773-154A=
|
NP_001127880.1:n.3773-154A=
|
|
XM_011522456.1:c.3803A=
|
XP_011520758.1:p.Glu1268=
|
|
XM_011522457.1:c.3704A=
|
XP_011520759.1:p.Glu1235=
|
|
XM_011522458.1:c.3491A=
|
XP_011520760.1:p.Glu1164=
|
|
XM_011522459.1:c.3491A=
|
XP_011520761.1:p.Glu1164=
|
|
XM_011522460.1:c.3491A=
|
XP_011520762.1:p.Glu1164=
|
|
XM_011522461.1:c.3773-154A=
|
XP_011520763.1:n.3773-154A=
|
|
XM_011522458.3:c.3491A=
|
XP_011520760.1:p.Glu1164=
|
|
XM_011522461.3:c.3773-154A=
|
XP_011520763.1:n.3773-154A=
|
|
XM_017023172.1:c.4118A=
|
XP_016878661.1:p.Glu1373=
|
|
XM_017023173.1:c.3929-154A=
|
XP_016878662.1:n.3929-154A=
|
|
NM_001134407.3:c.3962A=
MANE Select
|
NP_001127879.1:p.Glu1321=
|
|
NM_000833.5:c.3962A=
|
NP_000824.1:p.Glu1321=
|
|