ENST00000396043.4:c.*1095A>G
|
ENSP00000379358.4:n.*1095A>G
|
|
ENST00000374690.9:c.2747A>G
MANE Select
|
ENSP00000363822.3:p.Tyr916Cys
|
|
ENST00000396043.3:c.1374A>G
|
ENSP00000379358.3:n.1374A>G
|
|
ENST00000396044.8:c.*108A>G
|
ENSP00000379359.3:n.*108A>G
|
|
ENST00000612452.5:c.2747A>G
|
ENSP00000484033.2:p.Tyr916Cys
|
|
ENST00000374690.7:c.2747A>G
|
ENSP00000363822.3:p.Tyr916Cys
|
|
ENST00000396043.2:c.1151A>G
|
ENSP00000379358.2:p.Tyr384Cys
|
|
ENST00000396044.7:c.*108A>G
|
ENSP00000379359.3:n.*108A>G
|
|
ENST00000612452.4:c.2198A>G
|
ENSP00000484033.1:p.Tyr733Cys
|
|
NM_000044.3:c.2747A>G
|
NP_000035.2:p.Tyr916Cys
|
|
NM_001011645.2:c.1151A>G
|
NP_001011645.1:p.Tyr384Cys
|
|
NM_000044.4:c.2747A>G
|
NP_000035.2:p.Tyr916Cys
|
|
NM_001011645.3:c.1151A>G
|
NP_001011645.1:p.Tyr384Cys
|
|
NM_000044.6:c.2747A>G
MANE Select
|
NP_000035.2:p.Tyr916Cys
|
|