ENST00000228284.8:c.1823T>A
|
ENSP00000228284.4:p.Leu608His
|
|
ENST00000546815.6:c.1769T>A
MANE Select
|
ENSP00000449386.2:p.Leu590His
|
|
ENST00000651280.1:c.*925T>A
|
ENSP00000498612.1:n.*925T>A
|
|
ENST00000228284.7:c.1769T>A
|
ENSP00000228284.3:p.Leu590His
|
|
ENST00000431469.6:c.1661T>A
|
ENSP00000414453.2:p.Leu554His
|
|
ENST00000546728.5:c.*663T>A
|
ENSP00000449743.1:n.*663T>A
|
|
ENST00000546815.5:c.1823T>A
|
ENSP00000449386.1:p.Leu608His
|
|
ENST00000547528.5:c.*933T>A
|
ENSP00000446577.1:n.*933T>A
|
|
ENST00000548582.5:n.496T>A
|
|
|
ENST00000619503.4:n.705T>A
|
|
|
NM_014706.3:c.1769T>A
|
NP_055521.1:p.Leu590His
|
|
XM_005269241.3:c.1823T>A
|
XP_005269298.1:p.Leu608His
|
|
XM_011539026.1:c.905T>A
|
XP_011537328.1:p.Leu302His
|
|
NM_014706.4:c.1769T>A
MANE Select
|
NP_055521.1:p.Leu590His
|
|
XM_005269241.5:c.1823T>A
|
XP_005269298.1:p.Leu608His
|
|
XM_024449284.1:c.905T>A
|
XP_024305052.1:p.Leu302His
|
|