ENST00000350721.9:c.7812G>T
MANE Select
|
ENSP00000343741.4:p.Lys2604Asn
|
|
ENST00000513291.2:n.6521G>T
|
|
|
ENST00000653893.1:n.2670G>T
|
|
|
ENST00000654170.1:n.2655G>T
|
|
|
ENST00000656114.1:n.2898G>T
|
|
|
ENST00000656590.1:c.6739G>T
|
|
|
ENST00000658083.1:n.2992G>T
|
|
|
ENST00000661310.1:c.7620G>T
|
ENSP00000499589.1:p.Lys2540Asn
|
|
ENST00000665483.1:n.5352G>T
|
|
|
ENST00000666447.1:n.4315G>T
|
|
|
ENST00000666943.1:n.4544G>T
|
|
|
ENST00000350721.8:c.7812G>T
|
ENSP00000343741.4:p.Lys2604Asn
|
|
ENST00000504521.5:c.401G>T
|
ENSP00000422553.1:n.401G>T
|
|
ENST00000513291.1:c.4876G>T
|
|
|
ENST00000515810.1:c.238G>T
|
ENSP00000421870.1:n.238G>T
|
|
NM_001184.3:c.7812G>T
|
NP_001175.2:p.Lys2604Asn
|
|
XM_011512924.1:c.7818G>T
|
XP_011511226.1:p.Lys2606Asn
|
|
XM_011512925.1:c.7626G>T
|
XP_011511227.1:p.Lys2542Asn
|
|
XR_924147.1:n.10569G>T
|
|
|
XR_924148.1:n.8044G>T
|
|
|
NM_001354579.1:c.7620G>T
|
NP_001341508.1:p.Lys2540Asn
|
|
XR_001740179.2:n.8038G>T
|
|
|
XR_924148.2:n.8044G>T
|
|
|
NM_001184.4:c.7812G>T
MANE Select
|
NP_001175.2:p.Lys2604Asn
|
|
NM_001354579.2:c.7620G>T
|
NP_001341508.1:p.Lys2540Asn
|
|