ENST00000697337.1:c.*2592T>G
|
ENSP00000513259.1:n.*2592T>G
|
|
ENST00000697338.1:c.1704T>G
|
ENSP00000513260.1:n.1704T>G
|
|
ENST00000697339.1:c.890T>G
|
ENSP00000513261.1:p.Phe297Cys
|
|
ENST00000697340.1:c.*573T>G
|
ENSP00000513262.1:n.*573T>G
|
|
ENST00000697341.1:n.1826T>G
|
|
|
ENST00000313735.11:c.1856T>G
MANE Select
|
ENSP00000327251.6:p.Phe619Cys
|
|
ENST00000646938.1:c.1853T>G
|
ENSP00000494870.1:p.Phe618Cys
|
|
ENST00000313735.10:c.1856T>G
|
ENSP00000327251.6:p.Phe619Cys
|
|
ENST00000621962.1:c.1739T>G
|
ENSP00000482291.1:p.Phe580Cys
|
|
NM_000625.4:c.1856T>G
MANE Select
|
NP_000616.3:p.Phe619Cys
|
|
XM_011524859.1:c.1856T>G
|
XP_011523161.1:p.Phe619Cys
|
|
XM_011524860.1:c.1853T>G
|
XP_011523162.1:p.Phe618Cys
|
|
XM_011524861.1:c.1856T>G
|
XP_011523163.1:p.Phe619Cys
|
|
XM_011524862.1:c.1190T>G
|
XP_011523164.1:p.Phe397Cys
|
|