ENST00000282516.13:c.7728T>G
MANE Select
|
ENSP00000282516.8:p.Tyr2576Ter
|
|
ENST00000652901.1:c.7581T>G
|
ENSP00000499536.1:p.Tyr2527Ter
|
|
ENST00000282516.12:c.7728T>G
|
ENSP00000282516.8:p.Tyr2576Ter
|
|
ENST00000448238.2:c.7728T>G
|
ENSP00000406266.2:p.Tyr2576Ter
|
|
ENST00000513819.1:c.263+1721T>G
|
ENSP00000421504.1:n.263+1721T>G
|
|
ENST00000514335.1:n.1610T>G
|
|
|
ENST00000621733.1:c.1-3692T>G
|
ENSP00000480694.1:n.1-3692T>G
|
|
NM_015384.4:c.7728T>G
|
NP_056199.2:p.Tyr2576Ter
|
|
NM_133433.3:c.7728T>G
|
NP_597677.2:p.Tyr2576Ter
|
|
XM_005248280.2:c.7728T>G
|
XP_005248337.1:p.Tyr2576Ter
|
|
XM_005248282.3:c.6984T>G
|
XP_005248339.2:p.Tyr2328Ter
|
|
XM_006714467.2:c.7581T>G
|
XP_006714530.1:p.Tyr2527Ter
|
|
XM_006714468.1:c.7530T>G
|
XP_006714531.1:p.Tyr2510Ter
|
|
XM_011514014.1:c.7347T>G
|
XP_011512316.1:p.Tyr2449Ter
|
|
XM_011514015.1:c.*40T>G
|
XP_011512317.1:n.*40T>G
|
|
XM_005248280.3:c.7728T>G
|
XP_005248337.1:p.Tyr2576Ter
|
|
XM_005248282.5:c.7068T>G
|
XP_005248339.3:p.Tyr2356Ter
|
|
XM_006714468.2:c.7530T>G
|
XP_006714531.1:p.Tyr2510Ter
|
|
XM_017009329.1:c.7581T>G
|
XP_016864818.1:p.Tyr2527Ter
|
|
XM_017009330.2:c.6111T>G
|
XP_016864819.1:p.Tyr2037Ter
|
|
XM_017009331.1:c.6102T>G
|
XP_016864820.1:p.Tyr2034Ter
|
|
NM_133433.4:c.7728T>G
MANE Select
|
NP_597677.2:p.Tyr2576Ter
|
|
NM_015384.5:c.7728T>G
|
NP_056199.2:p.Tyr2576Ter
|
|