ENST00000645828.1:n.2594T>G
|
|
|
ENST00000651671.1:c.4787T>G
MANE Select
|
ENSP00000498587.1:p.Leu1596Arg
|
|
ENST00000679595.1:c.4787T>G
|
ENSP00000506241.1:p.Leu1596Arg
|
|
ENST00000680133.1:c.4673T>G
|
ENSP00000505319.1:p.Leu1558Arg
|
|
ENST00000680218.1:c.4667T>G
|
ENSP00000505339.1:p.Leu1556Arg
|
|
ENST00000680668.1:c.4673T>G
|
ENSP00000506336.1:p.Leu1558Arg
|
|
ENST00000680778.1:c.2384T>G
|
ENSP00000506033.1:p.Leu795Arg
|
|
ENST00000680924.1:c.*2187T>G
|
ENSP00000506031.1:n.*2187T>G
|
|
ENST00000681135.1:c.*2396T>G
|
ENSP00000506636.1:n.*2396T>G
|
|
ENST00000681298.1:n.1600T>G
|
|
|
ENST00000681454.1:c.*4023T>G
|
ENSP00000505763.1:n.*4023T>G
|
|
ENST00000277541.6:c.4787T>G
|
ENSP00000277541.6:p.Leu1596Arg
|
|
NM_017617.3:c.4787T>G
|
NP_060087.3:p.Leu1596Arg
|
|
XM_011518717.1:c.4088T>G
|
XP_011517019.1:p.Leu1363Arg
|
|
NM_017617.5:c.4787T>G
MANE Select
|
NP_060087.3:p.Leu1596Arg
|
|
XM_011518717.2:c.4064T>G
|
XP_011517019.2:p.Leu1355Arg
|
|