ENST00000278919.8:c.1072G>C
MANE Select
|
ENSP00000278919.3:p.Glu358Gln
|
|
ENST00000648911.1:c.1072G>C
|
ENSP00000497070.1:p.Glu358Gln
|
|
ENST00000278919.7:c.1072G>C
|
ENSP00000278919.3:p.Glu358Gln
|
|
ENST00000524427.5:n.585G>C
|
|
|
ENST00000527350.5:n.469G>C
|
|
|
ENST00000528863.5:n.280G>C
|
|
|
ENST00000530096.1:n.1571G>C
|
|
|
ENST00000532778.1:n.370G>C
|
|
|
NM_005103.4:c.1072G>C
|
NP_005094.1:p.Glu358Gln
|
|
XM_005271734.2:c.1072G>C
|
XP_005271791.1:p.Glu358Gln
|
|
XM_005271735.2:c.1072G>C
|
XP_005271792.1:p.Glu358Gln
|
|
NM_005103.5:c.1072G>C
MANE Select
|
NP_005094.1:p.Glu358Gln
|
|