ENST00000315491.12:c.985C>T
MANE Select
|
ENSP00000320295.7:p.Gln329Ter
|
|
ENST00000680788.1:n.4406C>T
|
|
|
ENST00000315491.11:c.985C>T
|
ENSP00000320295.7:p.Gln329Ter
|
|
ENST00000554444.5:c.769C>T
|
ENSP00000451617.1:p.Gln257Ter
|
|
ENST00000555576.5:c.277+1858C>T
|
ENSP00000452554.1:n.277+1858C>T
|
|
ENST00000555609.5:c.*1070C>T
|
ENSP00000451276.1:n.*1070C>T
|
|
ENST00000556922.1:c.2026C>T
|
ENSP00000451560.1:p.Gln676Ter
|
|
NM_001197181.1:c.769C>T
|
NP_001184110.1:p.Gln257Ter
|
|
NM_006086.3:c.985C>T
|
NP_006077.2:p.Gln329Ter
|
|
NM_006086.4:c.985C>T
MANE Select
|
NP_006077.2:p.Gln329Ter
|
|
NM_001197181.2:c.769C>T
|
NP_001184110.1:p.Gln257Ter
|
|