ENST00000474370.2:n.2426T>C
|
|
|
ENST00000492391.2:n.1577T>C
|
|
|
ENST00000682645.1:n.3524T>C
|
|
|
ENST00000683432.1:c.*628T>C
|
ENSP00000508174.1:n.*628T>C
|
|
ENST00000684207.1:c.453T>C
|
ENSP00000506942.1:p.His151=
|
|
ENST00000297157.8:c.453T>C
MANE Select
|
ENSP00000297157.3:p.His151=
|
|
ENST00000297157.7:c.453T>C
|
ENSP00000297157.3:p.His151=
|
|
ENST00000448915.1:c.351T>C
|
ENSP00000411577.1:p.His117=
|
|
NM_203288.1:c.453T>C
|
NP_976033.1:p.His151=
|
|
XM_011515468.1:c.351T>C
|
XP_011513770.1:p.His117=
|
|
XM_011515468.3:c.351T>C
|
XP_011513770.1:p.His117=
|
|
NM_203288.2:c.453T>C
MANE Select
|
NP_976033.1:p.His151=
|
|