ENST00000280362.8:c.249G>C
MANE Select
|
ENSP00000280362.3:p.Ala83=
|
|
ENST00000280362.7:c.249G>C
|
ENSP00000280362.3:p.Ala83=
|
|
ENST00000524931.1:c.45G>C
|
ENSP00000434688.1:p.Ala15=
|
|
ENST00000525803.1:c.169G>C
|
ENSP00000431750.1:p.Asp57His
|
|
ENST00000527428.5:n.423G>C
|
|
|
ENST00000527635.1:n.290G>C
|
|
|
ENST00000528679.5:c.*58G>C
|
ENSP00000435895.1:n.*58G>C
|
|
ENST00000531175.1:n.200G>C
|
|
|
ENST00000531673.5:c.*58G>C
|
ENSP00000433469.1:n.*58G>C
|
|
NM_000317.2:c.249G>C
|
NP_000308.1:p.Ala83=
|
|
XM_011542943.1:c.210G>C
|
XP_011541245.1:p.Ala70=
|
|
NM_000317.3:c.249G>C
MANE Select
|
NP_000308.1:p.Ala83=
|
|