ENST00000465218.3:n.666T>G
|
|
|
ENST00000468748.7:n.626T>G
|
|
|
ENST00000484154.2:n.1264T>G
|
|
|
ENST00000491008.6:n.1391T>G
|
|
|
ENST00000492226.2:n.640T>G
|
|
|
ENST00000492773.6:c.375T>G
|
|
|
ENST00000647636.1:c.643T>G
|
ENSP00000497505.1:p.Phe215Val
|
|
ENST00000647909.1:c.667T>G
|
ENSP00000498164.1:p.Phe223Val
|
|
ENST00000648145.1:c.411T>G
|
|
|
ENST00000648189.1:c.393T>G
|
|
|
ENST00000648256.1:c.592T>G
|
ENSP00000497356.1:p.Phe198Val
|
|
ENST00000648314.1:c.643T>G
|
ENSP00000496920.1:p.Phe215Val
|
|
ENST00000648599.1:c.643T>G
|
ENSP00000497159.1:p.Phe215Val
|
|
ENST00000648630.1:c.637T>G
|
ENSP00000497887.1:p.Phe213Val
|
|
ENST00000648682.1:c.643T>G
|
ENSP00000498185.1:p.Phe215Val
|
|
ENST00000648882.1:c.*469T>G
|
ENSP00000497603.1:n.*469T>G
|
|
ENST00000648890.1:c.643T>G
|
ENSP00000497503.1:p.Phe215Val
|
|
ENST00000648915.2:c.643T>G
MANE Select
|
ENSP00000497160.1:p.Phe215Val
|
|
ENST00000649545.1:c.377T>G
|
|
|
ENST00000649688.1:c.643T>G
|
ENSP00000497097.1:p.Phe215Val
|
|
ENST00000649814.1:n.692T>G
|
|
|
ENST00000650270.1:c.510T>G
|
|
|
ENST00000273783.7:c.643T>G
|
ENSP00000273783.3:p.Phe215Val
|
|
ENST00000432982.5:c.245+1359T>G
|
|
|
ENST00000444495.1:c.643T>G
|
ENSP00000409142.1:p.Phe215Val
|
|
ENST00000468748.5:n.96T>G
|
|
|
ENST00000481054.5:n.644T>G
|
|
|
ENST00000491008.5:n.607T>G
|
|
|
ENST00000491144.5:n.1083T>G
|
|
|
NM_003907.2:c.643T>G
|
NP_003898.2:p.Phe215Val
|
|
XR_924208.1:n.1594T>G
|
|
|
NM_003907.3:c.643T>G
MANE Select
|
NP_003898.2:p.Phe215Val
|
|
XM_011513266.3:c.-259T>G
|
XP_011511568.1:n.-259T>G
|
|
XR_001740352.2:n.1006T>G
|
|
|
XR_001740353.2:n.1006T>G
|
|
|
XR_924208.2:n.1006T>G
|
|
|