ENST00000330684.4:c.408T>A
MANE Select
|
ENSP00000332549.3:p.Ala136=
|
|
ENST00000637334.1:n.87T>A
|
|
|
ENST00000675189.1:n.892T>A
|
|
|
ENST00000675398.1:c.408T>A
|
ENSP00000502752.1:p.Ala136=
|
|
ENST00000676032.1:n.841T>A
|
|
|
ENST00000330684.3:c.408T>A
|
ENSP00000332549.3:p.Ala136=
|
|
ENST00000396573.6:c.408T>A
|
ENSP00000379818.2:p.Ala136=
|
|
ENST00000562109.5:c.408T>A
|
ENSP00000454998.1:p.Ala136=
|
|
ENST00000566665.1:n.809T>A
|
|
|
NM_000833.4:c.408T>A
|
NP_000824.1:p.Ala136=
|
|
NM_001134407.2:c.408T>A
|
NP_001127879.1:p.Ala136=
|
|
NM_001134408.2:c.408T>A
|
NP_001127880.1:p.Ala136=
|
|
XM_011522461.1:c.408T>A
|
XP_011520763.1:p.Ala136=
|
|
XM_011522461.3:c.408T>A
|
XP_011520763.1:p.Ala136=
|
|
XM_017023172.1:c.564T>A
|
XP_016878661.1:p.Ala188=
|
|
XM_017023173.1:c.564T>A
|
XP_016878662.1:p.Ala188=
|
|
NM_001134407.3:c.408T>A
MANE Select
|
NP_001127879.1:p.Ala136=
|
|
NM_000833.5:c.408T>A
|
NP_000824.1:p.Ala136=
|
|