ENST00000686218.1:c.*264T>C
|
ENSP00000509288.1:n.*264T>C
|
|
ENST00000648374.1:c.*264T>C
|
ENSP00000497255.1:n.*264T>C
|
|
ENST00000652429.1:c.*264T>C
MANE Select
|
ENSP00000498786.1:n.*264T>C
|
|
ENST00000278715.7:c.*264T>C
|
ENSP00000278715.3:n.*264T>C
|
|
ENST00000392841.1:c.*264T>C
|
ENSP00000376584.1:n.*264T>C
|
|
ENST00000544387.5:c.*264T>C
|
ENSP00000438424.1:n.*264T>C
|
|
ENST00000546226.5:n.2112T>C
|
|
|
NM_000190.3:c.*264T>C
|
NP_000181.2:n.*264T>C
|
|
NM_001024382.1:c.*264T>C
|
NP_001019553.1:n.*264T>C
|
|
NM_001258208.1:c.*264T>C
|
NP_001245137.1:n.*264T>C
|
|
NM_001258209.1:c.*264T>C
|
NP_001245138.1:n.*264T>C
|
|
XM_005271531.1:c.*264T>C
|
XP_005271588.1:n.*264T>C
|
|
XM_005271532.1:c.*264T>C
|
XP_005271589.1:n.*264T>C
|
|
XM_005271533.2:c.*264T>C
|
XP_005271590.1:n.*264T>C
|
|
XM_011542796.1:c.*264T>C
|
XP_011541098.1:n.*264T>C
|
|
NM_000190.4:c.*264T>C
MANE Select
|
NP_000181.2:n.*264T>C
|
|
NM_001024382.2:c.*264T>C
|
NP_001019553.1:n.*264T>C
|
|
XM_005271533.3:c.*264T>C
|
XP_005271590.1:n.*264T>C
|
|
XM_017017629.1:c.*264T>C
|
XP_016873118.1:n.*264T>C
|
|
XM_024448460.1:c.*264T>C
|
XP_024304228.1:n.*264T>C
|
|
NM_001258208.2:c.*264T>C
|
NP_001245137.1:n.*264T>C
|
|
NM_001258209.2:c.*264T>C
|
NP_001245138.1:n.*264T>C
|
|