ENST00000695651.1:n.1046A>G
|
|
|
ENST00000695652.1:c.2575A>G
|
ENSP00000512083.1:p.Ile859Val
|
|
ENST00000695653.1:c.607A>G
|
ENSP00000512084.1:p.Ile203Val
|
|
ENST00000695654.1:c.1822A>G
|
ENSP00000512085.1:p.Ile608Val
|
|
ENST00000695655.1:c.1639A>G
|
ENSP00000512086.1:n.1639A>G
|
|
ENST00000695692.1:n.2062A>G
|
|
|
ENST00000245907.11:c.2698A>G
MANE Select
|
ENSP00000245907.4:p.Ile900Val
|
|
ENST00000245907.10:c.2698A>G
|
ENSP00000245907.4:p.Ile900Val
|
|
ENST00000594005.1:n.274A>G
|
|
|
NM_000064.3:c.2698A>G
|
NP_000055.2:p.Ile900Val
|
|
NM_000064.4:c.2698A>G
MANE Select
|
NP_000055.2:p.Ile900Val
|
|