ENST00000380044.6:c.477A>T
MANE Select
|
ENSP00000369383.1:p.Gln159His
|
|
ENST00000233545.6:c.477A>T
|
ENSP00000233545.2:p.Gln159His
|
|
ENST00000357186.10:c.309A>T
|
ENSP00000349713.6:p.Gln103His
|
|
ENST00000380044.5:c.477A>T
|
ENSP00000369383.1:p.Gln159His
|
|
ENST00000402310.5:c.424A>T
|
ENSP00000383955.1:p.Met142Leu
|
|
ENST00000402722.5:c.*56A>T
|
ENSP00000386000.1:n.*56A>T
|
|
ENST00000405076.5:c.288A>T
|
ENSP00000385175.1:p.Gln96His
|
|
ENST00000405983.5:c.522A>T
|
ENSP00000384586.1:p.Gln174His
|
|
ENST00000415514.5:c.*278A>T
|
ENSP00000388043.1:n.*278A>T
|
|
ENST00000426513.6:c.*142A>T
|
ENSP00000403824.2:n.*142A>T
|
|
ENST00000430991.5:c.311A>T
|
|
|
ENST00000620797.4:n.150A>T
|
|
|
ENST00000621183.4:n.780A>T
|
|
|
NM_002437.4:c.477A>T
|
NP_002428.1:p.Gln159His
|
|
XM_005264326.2:c.477A>T
|
XP_005264383.1:p.Gln159His
|
|
XM_005264327.2:c.318A>T
|
XP_005264384.1:p.Gln106His
|
|
XM_006712021.2:c.429A>T
|
XP_006712084.1:p.Gln143His
|
|
XM_005264326.4:c.477A>T
|
XP_005264383.1:p.Gln159His
|
|
XM_006712021.3:c.429A>T
|
XP_006712084.1:p.Gln143His
|
|
XM_017004150.1:c.459A>T
|
XP_016859639.1:p.Gln153His
|
|
XM_017004151.1:c.429A>T
|
XP_016859640.1:p.Gln143His
|
|
XM_017004152.1:c.318A>T
|
XP_016859641.1:p.Gln106His
|
|
XM_024452913.1:c.429A>T
|
XP_024308681.1:p.Gln143His
|
|
NM_002437.5:c.477A>T
MANE Select
|
NP_002428.1:p.Gln159His
|
|