ENST00000573725.2:c.6822T>G
|
ENSP00000460849.2:p.Tyr2274Ter
|
|
ENST00000703537.1:c.2750T>G
|
|
|
ENST00000703538.1:c.*6725T>G
|
ENSP00000515361.1:n.*6725T>G
|
|
ENST00000703539.1:n.3316T>G
|
|
|
ENST00000703540.1:c.6855T>G
|
ENSP00000515362.1:p.Tyr2285Ter
|
|
ENST00000703541.1:c.6867T>G
|
ENSP00000515363.1:p.Tyr2289Ter
|
|
ENST00000304992.11:c.7002T>G
MANE Select
|
ENSP00000304350.6:p.Tyr2334Ter
|
|
ENST00000304992.10:c.7002T>G
|
ENSP00000304350.6:p.Tyr2334Ter
|
|
ENST00000571958.1:c.201T>G
|
|
|
ENST00000572621.5:c.7002T>G
|
ENSP00000460348.1:p.Tyr2334Ter
|
|
NM_006445.3:c.7002T>G
|
NP_006436.3:p.Tyr2334Ter
|
|
XM_024450537.1:c.7002T>G
|
XP_024306305.1:p.Tyr2334Ter
|
|
NM_006445.4:c.7002T>G
MANE Select
|
NP_006436.3:p.Tyr2334Ter
|
|