ENST00000474370.2:n.2392C>A
|
|
|
ENST00000492391.2:n.1543C>A
|
|
|
ENST00000682645.1:n.3490C>A
|
|
|
ENST00000683432.1:c.*594C>A
|
ENSP00000508174.1:n.*594C>A
|
|
ENST00000684207.1:c.419C>A
|
ENSP00000506942.1:p.Pro140His
|
|
ENST00000297157.8:c.419C>A
MANE Select
|
ENSP00000297157.3:p.Pro140His
|
|
ENST00000297157.7:c.419C>A
|
ENSP00000297157.3:p.Pro140His
|
|
ENST00000448915.1:c.317C>A
|
ENSP00000411577.1:p.Pro106His
|
|
NM_203288.1:c.419C>A
|
NP_976033.1:p.Pro140His
|
|
XM_011515468.1:c.317C>A
|
XP_011513770.1:p.Pro106His
|
|
XM_011515468.3:c.317C>A
|
XP_011513770.1:p.Pro106His
|
|
NM_203288.2:c.419C>A
MANE Select
|
NP_976033.1:p.Pro140His
|
|