|
NM_000343.4:c.1006C>T
MANE Select
|
NP_000334.1:p.Arg336Cys
|
|
ENST00000266088.9:c.1006C>T
MANE Select
|
ENSP00000266088.4:p.Arg336Cys
|
|
NM_000343.3:c.1006C>T
|
NP_000334.1:p.Arg336Cys
|
|
NM_001256314.1:c.625C>T
|
NP_001243243.1:p.Arg209Cys
|
|
NM_001256314.2:c.625C>T
|
NP_001243243.1:p.Arg209Cys
|
|
ENST00000266088.8:c.1006C>T
|
ENSP00000266088.4:p.Arg336Cys
|
|
ENST00000477969.1:n.172C>T
|
|
|
ENST00000486394.1:n.446C>T
|
|
|
ENST00000543737.2:c.625C>T
|
ENSP00000444898.1:p.Arg209Cys
|
|
XM_011530331.1:c.1006C>T
|
XP_011528633.1:p.Arg336Cys
|
|
XR_938173.1:n.592-16217G>A
|
|
|
XR_938174.1:n.487-16217G>A
|
|