ENST00000695651.1:n.2864T>G
|
|
|
ENST00000695653.1:c.2425T>G
|
ENSP00000512084.1:p.Cys809Gly
|
|
ENST00000695654.1:c.3541T>G
|
ENSP00000512085.1:p.Cys1181Gly
|
|
ENST00000695689.1:c.487T>G
|
ENSP00000512101.1:n.487T>G
|
|
ENST00000695690.1:n.1581T>G
|
|
|
ENST00000695691.1:n.1377T>G
|
|
|
ENST00000245907.11:c.4516T>G
MANE Select
|
ENSP00000245907.4:p.Cys1506Gly
|
|
ENST00000245907.10:c.4516T>G
|
ENSP00000245907.4:p.Cys1506Gly
|
|
ENST00000599668.1:n.111T>G
|
|
|
ENST00000599899.5:n.1475T>G
|
|
|
ENST00000601008.1:c.242-1479T>G
|
ENSP00000471384.1:n.242-1479T>G
|
|
NM_000064.3:c.4516T>G
|
NP_000055.2:p.Cys1506Gly
|
|
NM_000064.4:c.4516T>G
MANE Select
|
NP_000055.2:p.Cys1506Gly
|
|