ENST00000695651.1:n.1133C>G
|
|
|
ENST00000695652.1:c.2662C>G
|
ENSP00000512083.1:p.Leu888Val
|
|
ENST00000695653.1:c.694C>G
|
ENSP00000512084.1:p.Leu232Val
|
|
ENST00000695654.1:c.1909C>G
|
ENSP00000512085.1:p.Leu637Val
|
|
ENST00000695655.1:c.1726C>G
|
ENSP00000512086.1:n.1726C>G
|
|
ENST00000695692.1:n.2149C>G
|
|
|
ENST00000245907.11:c.2785C>G
MANE Select
|
ENSP00000245907.4:p.Leu929Val
|
|
ENST00000245907.10:c.2785C>G
|
ENSP00000245907.4:p.Leu929Val
|
|
ENST00000594005.1:n.361C>G
|
|
|
NM_000064.3:c.2785C>G
|
NP_000055.2:p.Leu929Val
|
|
NM_000064.4:c.2785C>G
MANE Select
|
NP_000055.2:p.Leu929Val
|
|