ENST00000642418.1:n.1539C>G
|
|
|
ENST00000643693.1:n.1003C>G
|
|
|
ENST00000644795.1:c.993C>G
|
ENSP00000495720.1:p.Leu331=
|
|
ENST00000646782.1:n.1935C>G
|
|
|
ENST00000647165.2:c.9201C>G
MANE Select
|
ENSP00000495481.1:p.Leu3067=
|
|
ENST00000651214.1:n.1706C>G
|
|
|
ENST00000205890.9:c.9201C>G
|
ENSP00000205890.5:p.Leu3067=
|
|
ENST00000418233.7:c.993C>G
|
ENSP00000408800.3:p.Leu331=
|
|
ENST00000433411.7:n.138C>G
|
|
|
ENST00000445289.6:n.316+1419C>G
|
|
|
ENST00000556535.5:c.63C>G
|
ENSP00000451782.1:p.Leu21=
|
|
ENST00000557190.5:n.103C>G
|
|
|
ENST00000557655.5:c.63C>G
|
ENSP00000451925.1:p.Leu21=
|
|
ENST00000578472.5:c.63C>G
|
ENSP00000467989.1:p.Leu21=
|
|
ENST00000615845.4:c.9201C>G
|
ENSP00000481642.1:p.Leu3067=
|
|
NM_016239.3:c.9201C>G
|
NP_057323.3:p.Leu3067=
|
|
XM_011523921.1:c.9195C>G
|
XP_011522223.1:p.Leu3065=
|
|
XM_017024714.2:c.9141C>G
|
XP_016880203.1:p.Leu3047=
|
|
XM_017024715.2:c.9204C>G
|
XP_016880204.1:p.Leu3068=
|
|
NM_016239.4:c.9201C>G
MANE Select
|
NP_057323.3:p.Leu3067=
|
|