ENST00000261837.12:c.335A>T
MANE Select
|
ENSP00000261837.7:p.Asp112Val
|
|
ENST00000261837.11:c.335A>T
|
ENSP00000261837.7:p.Asp112Val
|
|
ENST00000358784.11:c.209A>T
|
ENSP00000351635.7:p.Asp70Val
|
|
ENST00000396335.8:c.209A>T
|
ENSP00000379626.4:p.Asp70Val
|
|
ENST00000560075.1:n.366A>T
|
|
|
ENST00000560116.1:c.209A>T
|
ENSP00000453176.1:p.Asp70Val
|
|
ENST00000561313.5:c.209A>T
|
ENSP00000454185.1:p.Asp70Val
|
|
NM_006578.3:c.209A>T
|
NP_006569.1:p.Asp70Val
|
|
NM_016194.3:c.335A>T
|
NP_057278.2:p.Asp112Val
|
|
XM_011521162.1:c.209A>T
|
XP_011519464.1:p.Asp70Val
|
|
XM_011521163.1:c.53A>T
|
XP_011519465.1:p.Asp18Val
|
|
XM_011521162.3:c.209A>T
|
XP_011519464.1:p.Asp70Val
|
|
XM_011521163.3:c.53A>T
|
XP_011519465.1:p.Asp18Val
|
|
XR_001751060.2:n.287A>T
|
|
|
NM_006578.4:c.209A>T
|
NP_006569.1:p.Asp70Val
|
|
NM_016194.4:c.335A>T
MANE Select
|
NP_057278.2:p.Asp112Val
|
|
NM_001379343.1:c.53A>T
|
NP_001366272.1:p.Asp18Val
|
|