ENST00000282516.13:c.7728T=
MANE Select
|
ENSP00000282516.8:p.Tyr2576=
|
|
ENST00000652901.1:c.7581T=
|
ENSP00000499536.1:p.Tyr2527=
|
|
ENST00000282516.12:c.7728T=
|
ENSP00000282516.8:p.Tyr2576=
|
|
ENST00000448238.2:c.7728T=
|
ENSP00000406266.2:p.Tyr2576=
|
|
ENST00000513819.1:c.263+1721T=
|
ENSP00000421504.1:n.263+1721T=
|
|
ENST00000514335.1:n.1610T=
|
|
|
ENST00000621733.1:c.1-3692T=
|
ENSP00000480694.1:n.1-3692T=
|
|
NM_015384.4:c.7728T=
|
NP_056199.2:p.Tyr2576=
|
|
NM_133433.3:c.7728T=
|
NP_597677.2:p.Tyr2576=
|
|
XM_005248280.2:c.7728T=
|
XP_005248337.1:p.Tyr2576=
|
|
XM_005248282.3:c.6984T=
|
XP_005248339.2:p.Tyr2328=
|
|
XM_006714467.2:c.7581T=
|
XP_006714530.1:p.Tyr2527=
|
|
XM_006714468.1:c.7530T=
|
XP_006714531.1:p.Tyr2510=
|
|
XM_011514014.1:c.7347T=
|
XP_011512316.1:p.Tyr2449=
|
|
XM_011514015.1:c.*40T=
|
XP_011512317.1:n.*40T=
|
|
XM_005248280.3:c.7728T=
|
XP_005248337.1:p.Tyr2576=
|
|
XM_005248282.5:c.7068T=
|
XP_005248339.3:p.Tyr2356=
|
|
XM_006714468.2:c.7530T=
|
XP_006714531.1:p.Tyr2510=
|
|
XM_017009329.1:c.7581T=
|
XP_016864818.1:p.Tyr2527=
|
|
XM_017009330.2:c.6111T=
|
XP_016864819.1:p.Tyr2037=
|
|
XM_017009331.1:c.6102T=
|
XP_016864820.1:p.Tyr2034=
|
|
NM_133433.4:c.7728T=
MANE Select
|
NP_597677.2:p.Tyr2576=
|
|
NM_015384.5:c.7728T=
|
NP_056199.2:p.Tyr2576=
|
|