ENST00000209873.9:c.1072T>G
MANE Select
|
ENSP00000209873.4:p.Phe358Val
|
|
ENST00000546562.6:n.2136T>G
|
|
|
ENST00000547238.6:n.1708T>G
|
|
|
ENST00000547520.6:n.1066T>G
|
|
|
ENST00000547757.2:c.121T>G
|
ENSP00000448020.2:p.Phe41Val
|
|
ENST00000548880.2:n.1522T>G
|
|
|
ENST00000548931.6:c.592T>G
|
ENSP00000457518.1:p.Phe198Val
|
|
ENST00000549450.6:n.1006T>G
|
|
|
ENST00000552161.6:n.2028T>G
|
|
|
ENST00000672797.1:n.1561T>G
|
|
|
ENST00000672900.1:n.2014T>G
|
|
|
ENST00000209873.8:c.1072T>G
|
ENSP00000209873.4:p.Phe358Val
|
|
ENST00000394384.7:c.973T>G
|
ENSP00000377908.3:p.Phe325Val
|
|
ENST00000548931.5:c.592T>G
|
ENSP00000457518.1:p.Phe198Val
|
|
ENST00000550033.5:n.327T>G
|
|
|
ENST00000550286.5:c.700T>G
|
ENSP00000446885.1:p.Phe234Val
|
|
ENST00000552876.5:n.1415T>G
|
|
|
NM_001173466.1:c.973T>G
|
NP_001166937.1:p.Phe325Val
|
|
NM_015665.5:c.1072T>G
|
NP_056480.1:p.Phe358Val
|
|
XM_006719617.2:c.1087T>G
|
XP_006719680.1:p.Phe363Val
|
|
XM_011538777.1:c.1087T>G
|
XP_011537079.1:p.Phe363Val
|
|
XM_011538778.1:c.1072T>G
|
XP_011537080.1:p.Phe358Val
|
|
XM_011538779.1:c.988T>G
|
XP_011537081.1:p.Phe330Val
|
|
XM_011538780.1:c.973T>G
|
XP_011537082.1:p.Phe325Val
|
|
XM_011538781.1:c.421T>G
|
XP_011537083.1:p.Phe141Val
|
|
XM_011538778.2:c.1072T>G
|
XP_011537080.1:p.Phe358Val
|
|
XM_011538780.2:c.973T>G
|
XP_011537082.1:p.Phe325Val
|
|
XR_001748875.2:n.1129T>G
|
|
|
NM_015665.6:c.1072T>G
MANE Select
|
NP_056480.1:p.Phe358Val
|
|
NM_001173466.2:c.973T>G
|
NP_001166937.1:p.Phe325Val
|
|