ENST00000573725.2:c.6586T=
|
ENSP00000460849.2:p.Tyr2196=
|
|
ENST00000703537.1:c.2514T=
|
|
|
ENST00000703538.1:c.*6489T=
|
ENSP00000515361.1:n.*6489T=
|
|
ENST00000703539.1:n.3080T=
|
|
|
ENST00000703540.1:c.6619T=
|
ENSP00000515362.1:p.Tyr2207=
|
|
ENST00000703541.1:c.6631T=
|
ENSP00000515363.1:p.Tyr2211=
|
|
ENST00000304992.11:c.6766T=
MANE Select
|
ENSP00000304350.6:p.Tyr2256=
|
|
ENST00000304992.10:c.6766T=
|
ENSP00000304350.6:p.Tyr2256=
|
|
ENST00000571958.1:c.75T=
|
|
|
ENST00000572621.5:c.6766T=
|
ENSP00000460348.1:p.Tyr2256=
|
|
ENST00000572723.1:n.755T=
|
|
|
NM_006445.3:c.6766T=
|
NP_006436.3:p.Tyr2256=
|
|
XM_024450537.1:c.6766T=
|
XP_024306305.1:p.Tyr2256=
|
|
NM_006445.4:c.6766T=
MANE Select
|
NP_006436.3:p.Tyr2256=
|
|