ENST00000695651.1:n.2896G>C
|
|
|
ENST00000695653.1:c.2457G>C
|
ENSP00000512084.1:p.Glu819Asp
|
|
ENST00000695654.1:c.3573G>C
|
ENSP00000512085.1:p.Glu1191Asp
|
|
ENST00000695689.1:c.519G>C
|
ENSP00000512101.1:n.519G>C
|
|
ENST00000695690.1:n.1613G>C
|
|
|
ENST00000695691.1:n.1409G>C
|
|
|
ENST00000245907.11:c.4548G>C
MANE Select
|
ENSP00000245907.4:p.Glu1516Asp
|
|
ENST00000245907.10:c.4548G>C
|
ENSP00000245907.4:p.Glu1516Asp
|
|
ENST00000599668.1:n.168G>C
|
|
|
ENST00000599899.5:n.1507G>C
|
|
|
ENST00000601008.1:c.242-1249G>C
|
ENSP00000471384.1:n.242-1249G>C
|
|
NM_000064.3:c.4548G>C
|
NP_000055.2:p.Glu1516Asp
|
|
NM_000064.4:c.4548G>C
MANE Select
|
NP_000055.2:p.Glu1516Asp
|
|