|
ENST00000700029.2:c.643T>G
|
ENSP00000514759.2:p.Phe215Val
|
|
|
ENST00000710265.1:c.643T>G
|
ENSP00000518161.1:p.Phe215Val
|
|
|
ENST00000472832.3:c.643T>G
|
ENSP00000483066.2:p.Phe215Val
|
|
|
ENST00000688158.2:n.1378T>G
|
|
|
|
ENST00000688922.2:c.*473T>G
|
ENSP00000508742.2:n.*473T>G
|
|
|
ENST00000700021.1:c.598T>G
|
ENSP00000514757.1:p.Phe200Val
|
|
|
ENST00000700022.1:c.501T>G
|
ENSP00000514758.1:p.Ser167Arg
|
|
|
ENST00000700023.1:n.1801T>G
|
|
|
|
ENST00000700024.1:n.2035T>G
|
|
|
|
ENST00000700025.1:n.1412T>G
|
|
|
|
ENST00000700026.1:n.280T>G
|
|
|
|
ENST00000700029.1:c.477T>G
|
|
|
|
ENST00000706954.1:c.643T>G
|
ENSP00000516674.1:p.Phe215Val
|
|
|
ENST00000706955.1:c.*678T>G
|
ENSP00000516675.1:n.*678T>G
|
|
|
ENST00000686459.1:c.*229T>G
|
ENSP00000508909.1:n.*229T>G
|
|
|
ENST00000688158.1:c.*754T>G
|
ENSP00000509254.1:n.*754T>G
|
|
|
ENST00000688308.1:c.643T>G
|
ENSP00000508752.1:p.Phe215Val
|
|
|
ENST00000688922.1:c.564T>G
|
|
|
|
ENST00000693560.1:c.1162T>G
|
ENSP00000509861.1:p.Phe388Val
|
|
|
ENST00000371953.8:c.643T>G
MANE Select
|
ENSP00000361021.3:p.Phe215Val
|
|
|
ENST00000371953.7:c.643T>G
|
ENSP00000361021.3:p.Phe215Val
|
|
|
ENST00000472832.2:c.70T>G
|
ENSP00000483066.1:p.Phe24Val
|
|
|
NM_000314.5:c.643T>G
|
NP_000305.3:p.Phe215Val
|
|
|
NM_000314.6:c.643T>G
|
NP_000305.3:p.Phe215Val
|
|
|
NM_001304717.2:c.1162T>G
|
NP_001291646.2:p.Phe388Val
|
|
|
NM_001304718.1:c.52T>G
|
NP_001291647.1:p.Phe18Val
|
|
|
XM_006717926.2:c.598T>G
|
XP_006717989.1:p.Phe200Val
|
|
|
XM_011539981.1:c.643T>G
|
XP_011538283.1:p.Phe215Val
|
|
|
XM_011539982.1:c.547T>G
|
XP_011538284.1:p.Phe183Val
|
|
|
XR_945791.1:n.1213T>G
|
|
|
|
NM_000314.7:c.643T>G
|
NP_000305.3:p.Phe215Val
|
|
|
NM_001304717.5:c.1162T>G
|
NP_001291646.4:p.Phe388Val
|
|
|
NM_001304718.2:c.52T>G
|
NP_001291647.1:p.Phe18Val
|
|
|
NM_000314.8:c.643T>G
MANE Select
|
NP_000305.3:p.Phe215Val
|
|
