ENST00000698238.1:c.1672C>T
|
ENSP00000513620.1:p.Arg558Cys
|
|
ENST00000476941.6:c.1363C>T
MANE Select
|
ENSP00000419313.1:p.Arg455Cys
|
|
ENST00000273482.10:c.1261C>T
|
ENSP00000273482.6:p.Arg421Cys
|
|
ENST00000476941.5:c.1363C>T
|
ENSP00000419313.1:p.Arg455Cys
|
|
ENST00000612385.1:c.1261C>T
|
ENSP00000481537.1:p.Arg421Cys
|
|
NM_001251845.1:c.1363C>T
|
NP_001238774.1:p.Arg455Cys
|
|
NM_003304.4:c.1261C>T
|
NP_003295.1:p.Arg421Cys
|
|
XM_005247738.2:c.1069C>T
|
XP_005247795.1:p.Arg357Cys
|
|
XM_005247739.1:c.967C>T
|
XP_005247796.1:p.Arg323Cys
|
|
XR_241506.2:n.1825+6044C>T
|
|
|
XR_924164.1:n.1891C>T
|
|
|
XR_924165.1:n.1891C>T
|
|
|
XR_924166.1:n.1891C>T
|
|
|
XM_005247738.4:c.1069C>T
|
XP_005247795.1:p.Arg357Cys
|
|
XM_005247739.2:c.967C>T
|
XP_005247796.1:p.Arg323Cys
|
|
XM_017007121.2:c.1180C>T
|
XP_016862610.1:p.Arg394Cys
|
|
XR_001740246.1:n.2022C>T
|
|
|
XR_241506.4:n.1348+6044C>T
|
|
|
NM_001251845.2:c.1363C>T
MANE Select
|
NP_001238774.1:p.Arg455Cys
|
|
NM_003304.5:c.1261C>T
|
NP_003295.1:p.Arg421Cys
|
|