ENST00000474370.2:n.2399T>C
|
|
|
ENST00000492391.2:n.1550T>C
|
|
|
ENST00000682645.1:n.3497T>C
|
|
|
ENST00000683432.1:c.*601T>C
|
ENSP00000508174.1:n.*601T>C
|
|
ENST00000684207.1:c.426T>C
|
ENSP00000506942.1:p.Tyr142=
|
|
ENST00000297157.8:c.426T>C
MANE Select
|
ENSP00000297157.3:p.Tyr142=
|
|
ENST00000297157.7:c.426T>C
|
ENSP00000297157.3:p.Tyr142=
|
|
ENST00000448915.1:c.324T>C
|
ENSP00000411577.1:p.Tyr108=
|
|
NM_203288.1:c.426T>C
|
NP_976033.1:p.Tyr142=
|
|
XM_011515468.1:c.324T>C
|
XP_011513770.1:p.Tyr108=
|
|
XM_011515468.3:c.324T>C
|
XP_011513770.1:p.Tyr108=
|
|
NM_203288.2:c.426T>C
MANE Select
|
NP_976033.1:p.Tyr142=
|
|