ENST00000315491.12:c.853A=
MANE Select
|
ENSP00000320295.7:p.Thr285=
|
|
ENST00000680788.1:n.4274A=
|
|
|
ENST00000315491.11:c.853A=
|
ENSP00000320295.7:p.Thr285=
|
|
ENST00000554444.5:c.637A=
|
ENSP00000451617.1:p.Thr213=
|
|
ENST00000555576.5:c.277+1726A=
|
ENSP00000452554.1:n.277+1726A=
|
|
ENST00000555609.5:c.*938A=
|
ENSP00000451276.1:n.*938A=
|
|
ENST00000556922.1:c.1894A=
|
ENSP00000451560.1:p.Thr632=
|
|
NM_001197181.1:c.637A=
|
NP_001184110.1:p.Thr213=
|
|
NM_006086.3:c.853A=
|
NP_006077.2:p.Thr285=
|
|
NM_006086.4:c.853A=
MANE Select
|
NP_006077.2:p.Thr285=
|
|
NM_001197181.2:c.637A=
|
NP_001184110.1:p.Thr213=
|
|