ENST00000209873.9:c.1042T>G
MANE Select
|
ENSP00000209873.4:p.Leu348Val
|
|
ENST00000546562.6:n.2106T>G
|
|
|
ENST00000547238.6:n.1678T>G
|
|
|
ENST00000547520.6:n.1036T>G
|
|
|
ENST00000547757.2:c.91T>G
|
ENSP00000448020.2:p.Leu31Val
|
|
ENST00000548880.2:n.1492T>G
|
|
|
ENST00000548931.6:c.562T>G
|
ENSP00000457518.1:p.Leu188Val
|
|
ENST00000549450.6:n.976T>G
|
|
|
ENST00000552161.6:n.1998T>G
|
|
|
ENST00000672797.1:n.1531T>G
|
|
|
ENST00000672900.1:n.1984T>G
|
|
|
ENST00000209873.8:c.1042T>G
|
ENSP00000209873.4:p.Leu348Val
|
|
ENST00000394384.7:c.943T>G
|
ENSP00000377908.3:p.Leu315Val
|
|
ENST00000547520.5:n.746T>G
|
|
|
ENST00000548931.5:c.562T>G
|
ENSP00000457518.1:p.Leu188Val
|
|
ENST00000550033.5:n.297T>G
|
|
|
ENST00000550286.5:c.670T>G
|
ENSP00000446885.1:p.Leu224Val
|
|
ENST00000552876.5:n.1385T>G
|
|
|
NM_001173466.1:c.943T>G
|
NP_001166937.1:p.Leu315Val
|
|
NM_015665.5:c.1042T>G
|
NP_056480.1:p.Leu348Val
|
|
XM_006719617.2:c.1057T>G
|
XP_006719680.1:p.Leu353Val
|
|
XM_006719619.2:c.*52T>G
|
XP_006719682.1:n.*52T>G
|
|
XM_011538777.1:c.1057T>G
|
XP_011537079.1:p.Leu353Val
|
|
XM_011538778.1:c.1042T>G
|
XP_011537080.1:p.Leu348Val
|
|
XM_011538779.1:c.958T>G
|
XP_011537081.1:p.Leu320Val
|
|
XM_011538780.1:c.943T>G
|
XP_011537082.1:p.Leu315Val
|
|
XM_011538781.1:c.391T>G
|
XP_011537083.1:p.Leu131Val
|
|
XM_011538778.2:c.1042T>G
|
XP_011537080.1:p.Leu348Val
|
|
XM_011538780.2:c.943T>G
|
XP_011537082.1:p.Leu315Val
|
|
XR_001748875.2:n.1099T>G
|
|
|
NM_015665.6:c.1042T>G
MANE Select
|
NP_056480.1:p.Leu348Val
|
|
NM_001173466.2:c.943T>G
|
NP_001166937.1:p.Leu315Val
|
|