ENST00000330684.4:c.411C>T
MANE Select
|
ENSP00000332549.3:p.Asp137=
|
|
ENST00000637334.1:n.90C>T
|
|
|
ENST00000637393.1:c.3C>T
|
ENSP00000490232.1:p.Asp1=
|
|
ENST00000675189.1:n.895C>T
|
|
|
ENST00000675398.1:c.411C>T
|
ENSP00000502752.1:p.Asp137=
|
|
ENST00000676032.1:n.844C>T
|
|
|
ENST00000330684.3:c.411C>T
|
ENSP00000332549.3:p.Asp137=
|
|
ENST00000396573.6:c.411C>T
|
ENSP00000379818.2:p.Asp137=
|
|
ENST00000562109.5:c.411C>T
|
ENSP00000454998.1:p.Asp137=
|
|
ENST00000566665.1:n.812C>T
|
|
|
NM_000833.4:c.411C>T
|
NP_000824.1:p.Asp137=
|
|
NM_001134407.2:c.411C>T
|
NP_001127879.1:p.Asp137=
|
|
NM_001134408.2:c.411C>T
|
NP_001127880.1:p.Asp137=
|
|
XM_011522461.1:c.411C>T
|
XP_011520763.1:p.Asp137=
|
|
XM_011522461.3:c.411C>T
|
XP_011520763.1:p.Asp137=
|
|
XM_017023172.1:c.567C>T
|
XP_016878661.1:p.Asp189=
|
|
XM_017023173.1:c.567C>T
|
XP_016878662.1:p.Asp189=
|
|
NM_001134407.3:c.411C>T
MANE Select
|
NP_001127879.1:p.Asp137=
|
|
NM_000833.5:c.411C>T
|
NP_000824.1:p.Asp137=
|
|