ENST00000280362.8:c.291G>A
MANE Select
|
ENSP00000280362.3:p.Val97=
|
|
ENST00000280362.7:c.291G>A
|
ENSP00000280362.3:p.Val97=
|
|
ENST00000524931.1:c.87G>A
|
ENSP00000434688.1:p.Val29=
|
|
ENST00000525803.1:c.*25G>A
|
ENSP00000431750.1:n.*25G>A
|
|
ENST00000527428.5:n.465G>A
|
|
|
ENST00000527635.1:n.332G>A
|
|
|
ENST00000528679.5:c.*100G>A
|
ENSP00000435895.1:n.*100G>A
|
|
ENST00000531175.1:n.242G>A
|
|
|
ENST00000531673.5:c.*100G>A
|
ENSP00000433469.1:n.*100G>A
|
|
NM_000317.2:c.291G>A
|
NP_000308.1:p.Val97=
|
|
XM_011542943.1:c.252G>A
|
XP_011541245.1:p.Val84=
|
|
NM_000317.3:c.291G>A
MANE Select
|
NP_000308.1:p.Val97=
|
|