ENST00000315491.12:c.1189T>A
MANE Select
|
ENSP00000320295.7:p.Trp397Arg
|
|
ENST00000680788.1:n.4610T>A
|
|
|
ENST00000315491.11:c.1189T>A
|
ENSP00000320295.7:p.Trp397Arg
|
|
ENST00000554444.5:c.973T>A
|
ENSP00000451617.1:p.Trp325Arg
|
|
ENST00000555576.5:c.277+2062T>A
|
ENSP00000452554.1:n.277+2062T>A
|
|
ENST00000555609.5:c.*1274T>A
|
ENSP00000451276.1:n.*1274T>A
|
|
ENST00000556922.1:c.2230T>A
|
ENSP00000451560.1:p.Trp744Arg
|
|
NM_001197181.1:c.973T>A
|
NP_001184110.1:p.Trp325Arg
|
|
NM_006086.3:c.1189T>A
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NP_006077.2:p.Trp397Arg
|
|
NM_006086.4:c.1189T>A
MANE Select
|
NP_006077.2:p.Trp397Arg
|
|
NM_001197181.2:c.973T>A
|
NP_001184110.1:p.Trp325Arg
|
|