ENST00000330684.4:c.3950A>T
MANE Select
|
ENSP00000332549.3:p.Glu1317Val
|
|
ENST00000535259.6:c.3302-166A>T
|
ENSP00000441572.3:n.3302-166A>T
|
|
ENST00000636273.2:n.3366-166A>T
|
|
|
ENST00000674742.1:c.3479A>T
|
ENSP00000502200.1:p.Glu1160Val
|
|
ENST00000675398.1:c.*1320A>T
|
ENSP00000502752.1:n.*1320A>T
|
|
ENST00000330684.3:c.3950A>T
|
ENSP00000332549.3:p.Glu1317Val
|
|
ENST00000396573.6:c.3950A>T
|
ENSP00000379818.2:p.Glu1317Val
|
|
ENST00000396575.6:c.3539A>T
|
ENSP00000379820.3:p.Glu1180Val
|
|
ENST00000461292.3:n.3412-166A>T
|
|
|
ENST00000535259.5:c.3362-166A>T
|
ENSP00000441572.2:n.3362-166A>T
|
|
ENST00000562109.5:c.3773-166A>T
|
ENSP00000454998.1:n.3773-166A>T
|
|
NM_000833.4:c.3950A>T
|
NP_000824.1:p.Glu1317Val
|
|
NM_001134407.2:c.3950A>T
|
NP_001127879.1:p.Glu1317Val
|
|
NM_001134408.2:c.3773-166A>T
|
NP_001127880.1:n.3773-166A>T
|
|
XM_011522456.1:c.3791A>T
|
XP_011520758.1:p.Glu1264Val
|
|
XM_011522457.1:c.3692A>T
|
XP_011520759.1:p.Glu1231Val
|
|
XM_011522458.1:c.3479A>T
|
XP_011520760.1:p.Glu1160Val
|
|
XM_011522459.1:c.3479A>T
|
XP_011520761.1:p.Glu1160Val
|
|
XM_011522460.1:c.3479A>T
|
XP_011520762.1:p.Glu1160Val
|
|
XM_011522461.1:c.3773-166A>T
|
XP_011520763.1:n.3773-166A>T
|
|
XM_011522458.3:c.3479A>T
|
XP_011520760.1:p.Glu1160Val
|
|
XM_011522461.3:c.3773-166A>T
|
XP_011520763.1:n.3773-166A>T
|
|
XM_017023172.1:c.4106A>T
|
XP_016878661.1:p.Glu1369Val
|
|
XM_017023173.1:c.3929-166A>T
|
XP_016878662.1:n.3929-166A>T
|
|
NM_001134407.3:c.3950A>T
MANE Select
|
NP_001127879.1:p.Glu1317Val
|
|
NM_000833.5:c.3950A>T
|
NP_000824.1:p.Glu1317Val
|
|