ENST00000318471.5:c.787T>C
MANE Select
|
ENSP00000315680.3:p.Tyr263His
|
|
ENST00000541292.6:c.*52T>C
|
ENSP00000441004.1:n.*52T>C
|
|
ENST00000678002.1:c.475T>C
|
|
|
ENST00000678557.1:c.673T>C
|
ENSP00000502962.1:p.Tyr225His
|
|
ENST00000678593.1:c.792T>C
|
ENSP00000503841.1:n.792T>C
|
|
ENST00000679286.1:c.667T>C
|
ENSP00000503168.1:p.Tyr223His
|
|
ENST00000318471.4:c.787T>C
|
ENSP00000315680.3:p.Tyr263His
|
|
NM_000288.3:c.787T>C
|
NP_000279.1:p.Tyr263His
|
|
XM_005267019.3:c.673T>C
|
XP_005267076.1:p.Tyr225His
|
|
XM_006715502.1:c.493T>C
|
XP_006715565.1:p.Tyr165His
|
|
XM_011535900.1:c.527-25905T>C
|
XP_011534202.1:n.527-25905T>C
|
|
XM_005267019.4:c.673T>C
|
XP_005267076.1:p.Tyr225His
|
|
XM_006715502.2:c.493T>C
|
XP_006715565.1:p.Tyr165His
|
|
XM_017010934.2:c.527-25905T>C
|
XP_016866423.1:n.527-25905T>C
|
|
NM_000288.4:c.787T>C
MANE Select
|
NP_000279.1:p.Tyr263His
|
|