ENST00000315491.12:c.977T=
MANE Select
|
ENSP00000320295.7:p.Val326=
|
|
ENST00000680788.1:n.4398T=
|
|
|
ENST00000315491.11:c.977T=
|
ENSP00000320295.7:p.Val326=
|
|
ENST00000554444.5:c.761T=
|
ENSP00000451617.1:p.Val254=
|
|
ENST00000555576.5:c.277+1850T=
|
ENSP00000452554.1:n.277+1850T=
|
|
ENST00000555609.5:c.*1062T=
|
ENSP00000451276.1:n.*1062T=
|
|
ENST00000556922.1:c.2018T=
|
ENSP00000451560.1:p.Val673=
|
|
NM_001197181.1:c.761T=
|
NP_001184110.1:p.Val254=
|
|
NM_006086.3:c.977T=
|
NP_006077.2:p.Val326=
|
|
NM_006086.4:c.977T=
MANE Select
|
NP_006077.2:p.Val326=
|
|
NM_001197181.2:c.761T=
|
NP_001184110.1:p.Val254=
|
|