|
NM_000069.3:c.4972C>T
MANE Select
|
NP_000060.2:p.Arg1658Cys
|
|
ENST00000362061.4:c.4972C>T
MANE Select
|
ENSP00000355192.3:p.Arg1658Cys
|
|
NM_000069.2:c.4972C>T
|
NP_000060.2:p.Arg1658Cys
|
|
ENST00000362061.3:c.4972C>T
|
ENSP00000355192.3:p.Arg1658Cys
|
|
ENST00000367338.7:c.4915C>T
|
ENSP00000356307.3:p.Arg1639Cys
|
|
ENST00000679417.1:c.*4135C>T
|
ENSP00000506706.1:n.*4135C>T
|
|
ENST00000680051.1:n.2098C>T
|
|
|
ENST00000680059.1:c.*2490C>T
|
ENSP00000504944.1:n.*2490C>T
|
|
ENST00000681078.1:c.*747C>T
|
ENSP00000506645.1:n.*747C>T
|
|
ENST00000681190.1:c.*1154C>T
|
ENSP00000506428.1:n.*1154C>T
|
|
ENST00000681874.1:c.4912C>T
|
ENSP00000505162.1:p.Arg1638Cys
|
|
XM_005245478.2:c.4915C>T
|
XP_005245535.1:p.Arg1639Cys
|
|
XM_005245478.3:c.4915C>T
|
XP_005245535.1:p.Arg1639Cys
|