ENST00000534624.6:c.1549C>T
MANE Select
|
ENSP00000432083.1:p.Arg517Cys
|
|
ENST00000227378.7:c.1549C>T
|
ENSP00000227378.3:p.Arg517Cys
|
|
ENST00000453788.6:c.1387+309C>T
|
ENSP00000404372.2:n.1387+309C>T
|
|
ENST00000524552.5:c.322C>T
|
ENSP00000435908.1:p.Arg108Cys
|
|
ENST00000526110.5:c.1492C>T
|
ENSP00000433584.1:p.Arg498Cys
|
|
ENST00000526686.1:c.205C>T
|
ENSP00000435019.1:p.Arg69Cys
|
|
ENST00000532091.1:n.1671C>T
|
|
|
ENST00000532636.5:c.1549C>T
|
ENSP00000437125.1:p.Arg517Cys
|
|
ENST00000533540.5:c.1111C>T
|
ENSP00000437189.1:p.Arg371Cys
|
|
ENST00000534319.5:c.841C>T
|
ENSP00000433316.1:p.Arg281Cys
|
|
ENST00000534624.5:c.1549C>T
|
ENSP00000432083.1:p.Arg517Cys
|
|
NM_006597.5:c.1549C>T
|
NP_006588.1:p.Arg517Cys
|
|
NM_153201.3:c.1387+309C>T
|
NP_694881.1:n.1387+309C>T
|
|
XM_011542798.1:c.1549C>T
|
XP_011541100.1:p.Arg517Cys
|
|
NM_006597.6:c.1549C>T
MANE Select
|
NP_006588.1:p.Arg517Cys
|
|
NM_153201.4:c.1387+309C>T
|
NP_694881.1:n.1387+309C>T
|
|