ENST00000315491.12:c.849C>A
MANE Select
|
ENSP00000320295.7:p.Ala283=
|
|
ENST00000680788.1:n.4270C>A
|
|
|
ENST00000315491.11:c.849C>A
|
ENSP00000320295.7:p.Ala283=
|
|
ENST00000554444.5:c.633C>A
|
ENSP00000451617.1:p.Ala211=
|
|
ENST00000555576.5:c.277+1722C>A
|
ENSP00000452554.1:n.277+1722C>A
|
|
ENST00000555609.5:c.*934C>A
|
ENSP00000451276.1:n.*934C>A
|
|
ENST00000556922.1:c.1890C>A
|
ENSP00000451560.1:p.Ala630=
|
|
NM_001197181.1:c.633C>A
|
NP_001184110.1:p.Ala211=
|
|
NM_006086.3:c.849C>A
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NP_006077.2:p.Ala283=
|
|
NM_006086.4:c.849C>A
MANE Select
|
NP_006077.2:p.Ala283=
|
|
NM_001197181.2:c.633C>A
|
NP_001184110.1:p.Ala211=
|
|