ENST00000695651.1:n.2174T>G
|
|
|
ENST00000695653.1:c.1735T>G
|
ENSP00000512084.1:p.Phe579Val
|
|
ENST00000695654.1:c.2851T>G
|
ENSP00000512085.1:p.Phe951Val
|
|
ENST00000695690.1:n.17T>G
|
|
|
ENST00000695691.1:n.17T>G
|
|
|
ENST00000245907.11:c.3826T>G
MANE Select
|
ENSP00000245907.4:p.Phe1276Val
|
|
ENST00000245907.10:c.3826T>G
|
ENSP00000245907.4:p.Phe1276Val
|
|
ENST00000596238.1:n.269T>G
|
|
|
ENST00000601008.1:c.241+1615T>G
|
ENSP00000471384.1:n.241+1615T>G
|
|
NM_000064.3:c.3826T>G
|
NP_000055.2:p.Phe1276Val
|
|
NM_000064.4:c.3826T>G
MANE Select
|
NP_000055.2:p.Phe1276Val
|
|