ENST00000264012.9:c.876T>C
MANE Select
|
ENSP00000264012.4:p.Pro292=
|
|
ENST00000264012.8:c.876T>C
|
ENSP00000264012.4:p.Pro292=
|
|
ENST00000429102.6:c.876T>C
|
ENSP00000398485.2:p.Pro292=
|
|
ENST00000542274.5:c.*614T>C
|
ENSP00000464021.1:n.*614T>C
|
|
ENST00000569036.2:c.352T>C
|
|
|
NM_001793.4:c.876T>C
|
NP_001784.2:p.Pro292=
|
|
XM_011522800.1:c.876T>C
|
XP_011521102.1:p.Pro292=
|
|
NM_001317195.1:c.876T>C
|
NP_001304124.1:p.Pro292=
|
|
NM_001317196.1:c.711T>C
|
NP_001304125.1:p.Pro237=
|
|
NM_001793.5:c.876T>C
|
NP_001784.2:p.Pro292=
|
|
XM_011522800.3:c.876T>C
|
XP_011521102.1:p.Pro292=
|
|
NM_001793.6:c.876T>C
MANE Select
|
NP_001784.2:p.Pro292=
|
|
NM_001317195.2:c.876T>C
|
NP_001304124.1:p.Pro292=
|
|
NM_001317196.2:c.711T>C
|
NP_001304125.1:p.Pro237=
|
|
NM_001317195.3:c.876T>C
|
NP_001304124.1:p.Pro292=
|
|