ENST00000326003.7:c.691A>T
MANE Select
|
ENSP00000314151.1:p.Ser231Cys
|
|
ENST00000326003.6:c.691A>T
|
ENSP00000314151.1:p.Ser231Cys
|
|
ENST00000360617.7:c.1133A>T
|
ENSP00000353829.2:n.1133A>T
|
|
ENST00000422986.6:c.*347A>T
|
ENSP00000393628.2:n.*347A>T
|
|
ENST00000595392.5:c.*192A>T
|
ENSP00000468912.1:n.*192A>T
|
|
ENST00000595952.5:c.562A>T
|
ENSP00000471155.1:p.Ser188Cys
|
|
ENST00000596333.1:n.869A>T
|
|
|
ENST00000598145.1:c.693A>T
|
|
|
ENST00000601349.5:n.1970A>T
|
|
|
ENST00000601812.1:n.1123A>T
|
|
|
ENST00000617027.4:c.568A>T
|
ENSP00000483513.1:p.Ser190Cys
|
|
NM_001030047.1:c.*416A>T
|
NP_001025218.1:n.*416A>T
|
|
NM_001030048.1:c.562A>T
|
NP_001025219.1:p.Ser188Cys
|
|
NM_001648.2:c.691A>T
MANE Select
|
NP_001639.1:p.Ser231Cys
|
|
XM_011526923.1:c.709A>T
|
XP_011525225.1:p.Ser237Cys
|
|
XR_935817.1:n.1324+778A>T
|
|
|