ENST00000326003.7:c.786A>T
MANE Select
|
ENSP00000314151.1:p.Ter262Cys
|
|
ENST00000326003.6:c.786A>T
|
ENSP00000314151.1:p.Ter262Cys
|
|
ENST00000360617.7:c.1228A>T
|
ENSP00000353829.2:n.1228A>T
|
|
ENST00000422986.6:c.*442A>T
|
ENSP00000393628.2:n.*442A>T
|
|
ENST00000595392.5:c.*287A>T
|
ENSP00000468912.1:n.*287A>T
|
|
ENST00000595952.5:c.657A>T
|
ENSP00000471155.1:p.Ter219Cys
|
|
ENST00000596333.1:n.964A>T
|
|
|
ENST00000598145.1:c.788A>T
|
|
|
ENST00000601349.5:n.2065A>T
|
|
|
ENST00000601812.1:n.1218A>T
|
|
|
ENST00000617027.4:c.663A>T
|
ENSP00000483513.1:p.Ter221Cys
|
|
NM_001030047.1:c.*511A>T
|
NP_001025218.1:n.*511A>T
|
|
NM_001030048.1:c.657A>T
|
NP_001025219.1:p.Ter219Cys
|
|
NM_001648.2:c.786A>T
MANE Select
|
NP_001639.1:p.Ter262Cys
|
|
XM_011526923.1:c.804A>T
|
XP_011525225.1:p.Ter268Cys
|
|
XR_935817.1:n.1324+873A>T
|
|
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