ENST00000369538.4:c.374C>G
|
ENSP00000358551.4:p.Thr125Arg
|
|
ENST00000520113.7:c.386C>G
MANE Select
|
ENSP00000430075.3:p.Thr129Arg
|
|
ENST00000637080.1:c.389C>G
|
ENSP00000489753.1:p.Thr130Arg
|
|
ENST00000639077.1:n.51C>G
|
|
|
ENST00000369538.3:c.473C>G
|
ENSP00000358551.3:p.Thr158Arg
|
|
ENST00000485564.3:n.260C>G
|
|
|
ENST00000520113.6:c.485C>G
|
ENSP00000430075.2:p.Thr162Arg
|
|
NM_000036.2:c.485C>G
|
NP_000027.2:p.Thr162Arg
|
|
NM_001172626.1:c.473C>G
|
NP_001166097.1:p.Thr158Arg
|
|
NM_000036.3:c.386C>G
MANE Select
|
NP_000027.3:p.Thr129Arg
|
|
NM_001172626.2:c.374C>G
|
NP_001166097.2:p.Thr125Arg
|
|