ENST00000695651.1:n.2865G>C
|
|
|
ENST00000695653.1:c.2426G>C
|
ENSP00000512084.1:p.Cys809Ser
|
|
ENST00000695654.1:c.3542G>C
|
ENSP00000512085.1:p.Cys1181Ser
|
|
ENST00000695689.1:c.488G>C
|
ENSP00000512101.1:n.488G>C
|
|
ENST00000695690.1:n.1582G>C
|
|
|
ENST00000695691.1:n.1378G>C
|
|
|
ENST00000245907.11:c.4517G>C
MANE Select
|
ENSP00000245907.4:p.Cys1506Ser
|
|
ENST00000245907.10:c.4517G>C
|
ENSP00000245907.4:p.Cys1506Ser
|
|
ENST00000599668.1:n.112G>C
|
|
|
ENST00000599899.5:n.1476G>C
|
|
|
ENST00000601008.1:c.242-1478G>C
|
ENSP00000471384.1:n.242-1478G>C
|
|
NM_000064.3:c.4517G>C
|
NP_000055.2:p.Cys1506Ser
|
|
NM_000064.4:c.4517G>C
MANE Select
|
NP_000055.2:p.Cys1506Ser
|
|