ENST00000573725.2:c.6586T>C
|
ENSP00000460849.2:p.Tyr2196His
|
|
ENST00000703537.1:c.2514T>C
|
|
|
ENST00000703538.1:c.*6489T>C
|
ENSP00000515361.1:n.*6489T>C
|
|
ENST00000703539.1:n.3080T>C
|
|
|
ENST00000703540.1:c.6619T>C
|
ENSP00000515362.1:p.Tyr2207His
|
|
ENST00000703541.1:c.6631T>C
|
ENSP00000515363.1:p.Tyr2211His
|
|
ENST00000304992.11:c.6766T>C
MANE Select
|
ENSP00000304350.6:p.Tyr2256His
|
|
ENST00000304992.10:c.6766T>C
|
ENSP00000304350.6:p.Tyr2256His
|
|
ENST00000571958.1:c.75T>C
|
|
|
ENST00000572621.5:c.6766T>C
|
ENSP00000460348.1:p.Tyr2256His
|
|
ENST00000572723.1:n.755T>C
|
|
|
NM_006445.3:c.6766T>C
|
NP_006436.3:p.Tyr2256His
|
|
XM_024450537.1:c.6766T>C
|
XP_024306305.1:p.Tyr2256His
|
|
NM_006445.4:c.6766T>C
MANE Select
|
NP_006436.3:p.Tyr2256His
|
|