ENST00000318471.5:c.749T>G
MANE Select
|
ENSP00000315680.3:p.Phe250Cys
|
|
ENST00000541292.6:c.*14T>G
|
ENSP00000441004.1:n.*14T>G
|
|
ENST00000678002.1:c.437T>G
|
|
|
ENST00000678557.1:c.635T>G
|
ENSP00000502962.1:p.Phe212Cys
|
|
ENST00000678593.1:c.754T>G
|
ENSP00000503841.1:n.754T>G
|
|
ENST00000679286.1:c.629T>G
|
ENSP00000503168.1:p.Phe210Cys
|
|
ENST00000318471.4:c.749T>G
|
ENSP00000315680.3:p.Phe250Cys
|
|
NM_000288.3:c.749T>G
|
NP_000279.1:p.Phe250Cys
|
|
XM_005267019.3:c.635T>G
|
XP_005267076.1:p.Phe212Cys
|
|
XM_006715502.1:c.455T>G
|
XP_006715565.1:p.Phe152Cys
|
|
XM_011535900.1:c.527-25943T>G
|
XP_011534202.1:n.527-25943T>G
|
|
XM_005267019.4:c.635T>G
|
XP_005267076.1:p.Phe212Cys
|
|
XM_006715502.2:c.455T>G
|
XP_006715565.1:p.Phe152Cys
|
|
XM_017010934.2:c.527-25943T>G
|
XP_016866423.1:n.527-25943T>G
|
|
NM_000288.4:c.749T>G
MANE Select
|
NP_000279.1:p.Phe250Cys
|
|