ENST00000262367.10:c.4034T>A
MANE Select
|
ENSP00000262367.5:p.Phe1345Tyr
|
|
ENST00000262367.9:c.4034T>A
|
ENSP00000262367.5:p.Phe1345Tyr
|
|
ENST00000382070.7:c.3920T>A
|
ENSP00000371502.3:p.Phe1307Tyr
|
|
ENST00000570939.2:c.2669T>A
|
ENSP00000461002.2:p.Phe890Tyr
|
|
ENST00000572569.1:n.498T>A
|
|
|
ENST00000573517.6:c.340T>A
|
|
|
ENST00000574740.1:n.116T>A
|
|
|
ENST00000576720.1:n.2971T>A
|
|
|
NM_001079846.1:c.3920T>A
|
NP_001073315.1:p.Phe1307Tyr
|
|
NM_004380.2:c.4034T>A
|
NP_004371.2:p.Phe1345Tyr
|
|
XM_005255124.3:c.3989T>A
|
XP_005255181.1:p.Phe1330Tyr
|
|
XM_005255125.3:c.3617T>A
|
XP_005255182.1:p.Phe1206Tyr
|
|
XM_006720848.2:c.4034T>A
|
XP_006720911.1:p.Phe1345Tyr
|
|
XM_011522380.1:c.3980T>A
|
XP_011520682.1:p.Phe1327Tyr
|
|
XM_011522381.1:c.3281T>A
|
XP_011520683.1:p.Phe1094Tyr
|
|
XM_005255124.4:c.3989T>A
|
XP_005255181.1:p.Phe1330Tyr
|
|
XM_005255125.4:c.3617T>A
|
XP_005255182.1:p.Phe1206Tyr
|
|
XM_006720848.3:c.4034T>A
|
XP_006720911.1:p.Phe1345Tyr
|
|
XM_011522381.2:c.3281T>A
|
XP_011520683.1:p.Phe1094Tyr
|
|
XM_017022944.1:c.4028T>A
|
XP_016878433.1:p.Phe1343Tyr
|
|
NM_004380.3:c.4034T>A
MANE Select
|
NP_004371.2:p.Phe1345Tyr
|
|