ENST00000697337.1:c.*2562T>G
|
ENSP00000513259.1:n.*2562T>G
|
|
ENST00000697338.1:c.1674T>G
|
ENSP00000513260.1:n.1674T>G
|
|
ENST00000697339.1:c.860T>G
|
ENSP00000513261.1:p.Leu287Arg
|
|
ENST00000697340.1:c.*543T>G
|
ENSP00000513262.1:n.*543T>G
|
|
ENST00000697341.1:n.1796T>G
|
|
|
ENST00000313735.11:c.1826T>G
MANE Select
|
ENSP00000327251.6:p.Leu609Arg
|
|
ENST00000646938.1:c.1823T>G
|
ENSP00000494870.1:p.Leu608Arg
|
|
ENST00000313735.10:c.1826T>G
|
ENSP00000327251.6:p.Leu609Arg
|
|
ENST00000621962.1:c.1709T>G
|
ENSP00000482291.1:p.Leu570Arg
|
|
NM_000625.4:c.1826T>G
MANE Select
|
NP_000616.3:p.Leu609Arg
|
|
XM_011524859.1:c.1826T>G
|
XP_011523161.1:p.Leu609Arg
|
|
XM_011524860.1:c.1823T>G
|
XP_011523162.1:p.Leu608Arg
|
|
XM_011524861.1:c.1826T>G
|
XP_011523163.1:p.Leu609Arg
|
|
XM_011524862.1:c.1160T>G
|
XP_011523164.1:p.Leu387Arg
|
|