ENST00000352909.8:c.764T>G
MANE Select
|
ENSP00000325951.4:p.Phe255Cys
|
|
ENST00000324155.8:c.*453T>G
|
ENSP00000325831.3:n.*453T>G
|
|
ENST00000333684.9:c.696-415T>G
|
ENSP00000328814.6:n.696-415T>G
|
|
ENST00000352909.7:c.764T>G
|
ENSP00000325951.3:p.Phe255Cys
|
|
ENST00000381168.7:c.*484T>G
|
ENSP00000370560.3:n.*484T>G
|
|
ENST00000381175.5:c.845T>G
|
ENSP00000370567.1:p.Phe282Cys
|
|
ENST00000381178.5:c.857T>G
|
ENSP00000370571.1:p.Phe286Cys
|
|
ENST00000412076.1:c.136-415T>G
|
|
|
ENST00000416223.5:c.136-196T>G
|
|
|
ENST00000469226.1:n.893T>G
|
|
|
ENST00000479437.5:n.313T>G
|
|
|
NM_000360.3:c.764T>G
|
NP_000351.2:p.Phe255Cys
|
|
NM_199292.2:c.857T>G
|
NP_954986.2:p.Phe286Cys
|
|
NM_199293.2:c.845T>G
|
NP_954987.2:p.Phe282Cys
|
|
XM_011520335.1:c.776T>G
|
XP_011518637.1:p.Phe259Cys
|
|
XM_011520335.2:c.776T>G
|
XP_011518637.1:p.Phe259Cys
|
|
NM_000360.4:c.764T>G
MANE Select
|
NP_000351.2:p.Phe255Cys
|
|
NM_199292.3:c.857T>G
|
NP_954986.2:p.Phe286Cys
|
|
NM_199293.3:c.845T>G
|
NP_954987.2:p.Phe282Cys
|
|