ENST00000330684.4:c.953C>T
MANE Select
|
ENSP00000332549.3:p.Ala318Val
|
|
ENST00000535259.6:c.482C>T
|
ENSP00000441572.3:p.Ala161Val
|
|
ENST00000636273.2:n.546C>T
|
|
|
ENST00000637393.1:c.545C>T
|
ENSP00000490232.1:p.Ala182Val
|
|
ENST00000674742.1:c.482C>T
|
ENSP00000502200.1:p.Ala161Val
|
|
ENST00000675189.1:n.1437C>T
|
|
|
ENST00000675398.1:c.953C>T
|
ENSP00000502752.1:p.Ala318Val
|
|
ENST00000330684.3:c.953C>T
|
ENSP00000332549.3:p.Ala318Val
|
|
ENST00000396573.6:c.953C>T
|
ENSP00000379818.2:p.Ala318Val
|
|
ENST00000396575.6:c.542C>T
|
ENSP00000379820.3:p.Ala181Val
|
|
ENST00000461292.3:n.592C>T
|
|
|
ENST00000535259.5:c.542C>T
|
ENSP00000441572.2:p.Ala181Val
|
|
ENST00000562109.5:c.953C>T
|
ENSP00000454998.1:p.Ala318Val
|
|
ENST00000566683.1:n.241-46913C>T
|
|
|
ENST00000568247.3:n.845C>T
|
|
|
NM_000833.4:c.953C>T
|
NP_000824.1:p.Ala318Val
|
|
NM_001134407.2:c.953C>T
|
NP_001127879.1:p.Ala318Val
|
|
NM_001134408.2:c.953C>T
|
NP_001127880.1:p.Ala318Val
|
|
XM_011522456.1:c.794C>T
|
XP_011520758.1:p.Ala265Val
|
|
XM_011522457.1:c.695C>T
|
XP_011520759.1:p.Ala232Val
|
|
XM_011522458.1:c.482C>T
|
XP_011520760.1:p.Ala161Val
|
|
XM_011522459.1:c.482C>T
|
XP_011520761.1:p.Ala161Val
|
|
XM_011522460.1:c.482C>T
|
XP_011520762.1:p.Ala161Val
|
|
XM_011522461.1:c.953C>T
|
XP_011520763.1:p.Ala318Val
|
|
XM_011522458.3:c.482C>T
|
XP_011520760.1:p.Ala161Val
|
|
XM_011522461.3:c.953C>T
|
XP_011520763.1:p.Ala318Val
|
|
XM_017023172.1:c.1109C>T
|
XP_016878661.1:p.Ala370Val
|
|
XM_017023173.1:c.1109C>T
|
XP_016878662.1:p.Ala370Val
|
|
NM_001134407.3:c.953C>T
MANE Select
|
NP_001127879.1:p.Ala318Val
|
|
NM_000833.5:c.953C>T
|
NP_000824.1:p.Ala318Val
|
|