ENST00000398603.6:c.352T=
|
ENSP00000381604.1:p.Tyr118=
|
|
ENST00000398606.10:c.460T=
MANE Select
|
ENSP00000381607.3:p.Tyr154=
|
|
ENST00000646888.1:c.*176T=
|
ENSP00000494477.1:n.*176T=
|
|
ENST00000398603.5:c.352T=
|
ENSP00000381604.1:p.Tyr118=
|
|
ENST00000398606.7:c.460T=
|
ENSP00000381607.3:p.Tyr154=
|
|
ENST00000467591.1:n.571T=
|
|
|
ENST00000494593.1:n.1432T=
|
|
|
ENST00000495996.1:c.186T=
|
ENSP00000484686.1:p.Thr62=
|
|
ENST00000498765.5:c.523T=
|
|
|
NM_000852.3:c.460T= , LRG_723t1:c.460T=
|
NP_000843.1:p.Tyr154=
|
|
NM_000852.4:c.460T=
MANE Select
|
NP_000843.1:p.Tyr154=
|
|