ENST00000686218.1:c.524A>G
|
ENSP00000509288.1:p.Asp175Gly
|
|
ENST00000691144.1:n.2670A>G
|
|
|
ENST00000691249.1:n.1513A>G
|
|
|
ENST00000442944.7:c.671A>G
|
ENSP00000392041.3:p.Asp224Gly
|
|
ENST00000536813.6:c.638A>G
|
ENSP00000438726.2:p.Asp213Gly
|
|
ENST00000640813.1:c.499A>G
|
ENSP00000491061.1:p.Thr167Ala
|
|
ENST00000648026.1:c.583A>G
|
ENSP00000498044.1:p.Thr195Ala
|
|
ENST00000648374.1:c.638A>G
|
ENSP00000497255.1:p.Asp213Gly
|
|
ENST00000649823.1:n.1146A>G
|
|
|
ENST00000650101.1:c.620A>G
|
ENSP00000496970.1:p.Asp207Gly
|
|
ENST00000650307.1:n.1515A>G
|
|
|
ENST00000652429.1:c.689A>G
MANE Select
|
ENSP00000498786.1:p.Asp230Gly
|
|
ENST00000278715.7:c.689A>G
|
ENSP00000278715.3:p.Asp230Gly
|
|
ENST00000392841.1:c.638A>G
|
ENSP00000376584.1:p.Asp213Gly
|
|
ENST00000442944.6:c.638A>G
|
ENSP00000392041.2:p.Asp213Gly
|
|
ENST00000537841.5:c.638A>G
|
ENSP00000444730.1:p.Asp213Gly
|
|
ENST00000542044.5:n.1134A>G
|
|
|
ENST00000542729.5:c.600+278A>G
|
ENSP00000443058.1:n.600+278A>G
|
|
ENST00000543090.5:c.596A>G
|
ENSP00000445429.1:p.Asp199Gly
|
|
ENST00000543543.5:n.1164A>G
|
|
|
ENST00000544182.1:n.904A>G
|
|
|
ENST00000544387.5:c.651+278A>G
|
ENSP00000438424.1:n.651+278A>G
|
|
ENST00000545621.5:c.*824A>G
|
ENSP00000444849.1:n.*824A>G
|
|
ENST00000546226.5:n.1217A>G
|
|
|
NM_000190.3:c.689A>G
|
NP_000181.2:p.Asp230Gly
|
|
NM_001024382.1:c.638A>G
|
NP_001019553.1:p.Asp213Gly
|
|
NM_001258208.1:c.651+278A>G
|
NP_001245137.1:n.651+278A>G
|
|
NM_001258209.1:c.600+278A>G
|
NP_001245138.1:n.600+278A>G
|
|
XM_005271531.1:c.638A>G
|
XP_005271588.1:p.Asp213Gly
|
|
XM_005271532.1:c.638A>G
|
XP_005271589.1:p.Asp213Gly
|
|
XM_005271533.2:c.635A>G
|
XP_005271590.1:p.Asp212Gly
|
|
XM_011542796.1:c.524A>G
|
XP_011541098.1:p.Asp175Gly
|
|
NM_000190.4:c.689A>G
MANE Select
|
NP_000181.2:p.Asp230Gly
|
|
NM_001024382.2:c.638A>G
|
NP_001019553.1:p.Asp213Gly
|
|
XM_005271533.3:c.635A>G
|
XP_005271590.1:p.Asp212Gly
|
|
XM_017017629.1:c.638A>G
|
XP_016873118.1:p.Asp213Gly
|
|
XM_024448460.1:c.597+278A>G
|
XP_024304228.1:n.597+278A>G
|
|
NM_001258208.2:c.651+278A>G
|
NP_001245137.1:n.651+278A>G
|
|
NM_001258209.2:c.600+278A>G
|
NP_001245138.1:n.600+278A>G
|
|