ENST00000396705.10:c.545C>T
MANE Select
|
ENSP00000379933.4:p.Ala182Val
|
|
ENST00000229270.8:c.656C>T
|
ENSP00000229270.4:p.Ala219Val
|
|
ENST00000396705.9:c.545C>T
|
ENSP00000379933.4:p.Ala182Val
|
|
ENST00000474253.1:n.34C>T
|
|
|
ENST00000482209.1:n.241C>T
|
|
|
ENST00000488464.6:c.299C>T
|
ENSP00000475620.1:p.Ala100Val
|
|
ENST00000493987.5:c.299C>T
|
ENSP00000475364.1:p.Ala100Val
|
|
ENST00000535434.5:c.299C>T
|
ENSP00000443599.1:p.Ala100Val
|
|
ENST00000613953.4:c.656C>T
|
ENSP00000484435.1:p.Ala219Val
|
|
NM_000365.5:c.545C>T
|
NP_000356.1:p.Ala182Val
|
|
NM_001159287.1:c.656C>T
|
NP_001152759.1:p.Ala219Val
|
|
NM_001258026.1:c.299C>T
|
NP_001244955.1:p.Ala100Val
|
|
XR_002957378.1:n.1553C>T
|
|
|
NM_000365.6:c.545C>T
MANE Select
|
NP_000356.1:p.Ala182Val
|
|
NM_001258026.2:c.299C>T
|
NP_001244955.1:p.Ala100Val
|
|