ENST00000474370.2:n.2393C>T
|
|
|
ENST00000492391.2:n.1544C>T
|
|
|
ENST00000682645.1:n.3491C>T
|
|
|
ENST00000683432.1:c.*595C>T
|
ENSP00000508174.1:n.*595C>T
|
|
ENST00000684207.1:c.420C>T
|
ENSP00000506942.1:p.Pro140=
|
|
ENST00000297157.8:c.420C>T
MANE Select
|
ENSP00000297157.3:p.Pro140=
|
|
ENST00000297157.7:c.420C>T
|
ENSP00000297157.3:p.Pro140=
|
|
ENST00000448915.1:c.318C>T
|
ENSP00000411577.1:p.Pro106=
|
|
NM_203288.1:c.420C>T
|
NP_976033.1:p.Pro140=
|
|
XM_011515468.1:c.318C>T
|
XP_011513770.1:p.Pro106=
|
|
XM_011515468.3:c.318C>T
|
XP_011513770.1:p.Pro106=
|
|
NM_203288.2:c.420C>T
MANE Select
|
NP_976033.1:p.Pro140=
|
|