ENST00000542639.6:c.435T>C
|
ENSP00000440846.1:p.Thr145=
|
|
ENST00000686683.1:c.144T>C
|
ENSP00000509063.1:p.Thr48=
|
|
ENST00000686980.1:n.966T>C
|
|
|
ENST00000688006.1:c.435T>C
|
ENSP00000510311.1:p.Thr145=
|
|
ENST00000688859.1:n.390T>C
|
|
|
ENST00000689087.1:c.435T>C
|
ENSP00000508997.1:p.Thr145=
|
|
ENST00000693128.1:c.729T>C
|
ENSP00000508493.1:p.Thr243=
|
|
ENST00000338702.4:c.834T>C
MANE Select
|
ENSP00000340684.3:p.Thr278=
|
|
ENST00000338702.3:c.834T>C
|
ENSP00000340684.3:p.Thr278=
|
|
ENST00000542639.5:c.435T>C
|
ENSP00000440846.1:p.Thr145=
|
|
NM_000240.3:c.834T>C
|
NP_000231.1:p.Thr278=
|
|
NM_001270458.1:c.435T>C
|
NP_001257387.1:p.Thr145=
|
|
NM_000240.4:c.834T>C
MANE Select
|
NP_000231.1:p.Thr278=
|
|
NM_001270458.2:c.435T>C
|
NP_001257387.1:p.Thr145=
|
|