ENST00000695651.1:n.901C>G
|
|
|
ENST00000695652.1:c.2430C>G
|
ENSP00000512083.1:p.Leu810=
|
|
ENST00000695653.1:c.462C>G
|
ENSP00000512084.1:p.Leu154=
|
|
ENST00000695654.1:c.1677C>G
|
ENSP00000512085.1:p.Leu559=
|
|
ENST00000695655.1:c.1494C>G
|
ENSP00000512086.1:n.1494C>G
|
|
ENST00000695692.1:n.1917C>G
|
|
|
ENST00000245907.11:c.2553C>G
MANE Select
|
ENSP00000245907.4:p.Leu851=
|
|
ENST00000245907.10:c.2553C>G
|
ENSP00000245907.4:p.Leu851=
|
|
ENST00000594005.1:n.34C>G
|
|
|
ENST00000602053.1:n.601C>G
|
|
|
NM_000064.3:c.2553C>G
|
NP_000055.2:p.Leu851=
|
|
NM_000064.4:c.2553C>G
MANE Select
|
NP_000055.2:p.Leu851=
|
|