|
ENST00000473665.2:n.5922T>G
|
|
|
|
ENST00000482662.2:n.4329T>G
|
|
|
|
ENST00000685865.1:n.2281T>G
|
|
|
|
ENST00000687250.1:n.1981T>G
|
|
|
|
ENST00000687995.1:n.1796T>G
|
|
|
|
ENST00000688205.1:c.*1037T>G
|
ENSP00000509673.1:n.*1037T>G
|
|
|
ENST00000688788.1:n.1683T>G
|
|
|
|
ENST00000689276.1:c.1375T>G
|
ENSP00000510012.1:p.Phe459Val
|
|
|
ENST00000689576.1:c.*63T>G
|
ENSP00000508712.1:n.*63T>G
|
|
|
ENST00000690108.1:c.*1100T>G
|
ENSP00000510617.1:n.*1100T>G
|
|
|
ENST00000690468.1:c.1013T>G
|
ENSP00000509078.1:p.Phe338Cys
|
|
|
ENST00000690595.1:c.769T>G
|
ENSP00000508979.1:p.Phe257Val
|
|
|
ENST00000691348.1:c.1121T>G
|
ENSP00000509369.1:p.Phe374Cys
|
|
|
ENST00000691410.1:c.*1021T>G
|
ENSP00000508479.1:n.*1021T>G
|
|
|
ENST00000693287.1:c.760T>G
|
ENSP00000510264.1:p.Phe254Val
|
|
|
ENST00000693681.1:c.757T>G
|
ENSP00000510789.1:p.Phe253Val
|
|
|
ENST00000233838.9:c.1444T>G
MANE Select
|
ENSP00000233838.3:p.Phe482Val
|
|
|
ENST00000233838.8:c.1444T>G
|
ENSP00000233838.3:p.Phe482Val
|
|
|
ENST00000430215.7:c.1273T>G
|
ENSP00000408045.3:p.Phe425Val
|
|
|
ENST00000465637.5:n.179-3973T>G
|
|
|
|
NM_000821.5:c.1444T>G
|
NP_000812.2:p.Phe482Val
|
|
|
NM_000821.6:c.1444T>G
|
NP_000812.2:p.Phe482Val
|
|
|
NM_001142269.2:c.1273T>G
|
NP_001135741.1:p.Phe425Val
|
|
|
NM_001142269.3:c.1273T>G
|
NP_001135741.1:p.Phe425Val
|
|
|
XM_005264259.3:c.1444T>G
|
XP_005264316.1:p.Phe482Val
|
|
|
XM_011532764.1:c.622T>G
|
XP_011531066.1:p.Phe208Val
|
|
|
XM_011532765.1:c.622T>G
|
XP_011531067.1:p.Phe208Val
|
|
|
XR_939677.1:n.1357T>G
|
|
|
|
XM_005264259.5:c.1444T>G
|
XP_005264316.1:p.Phe482Val
|
|
|
XM_011532764.3:c.622T>G
|
XP_011531066.1:p.Phe208Val
|
|
|
XM_011532765.3:c.622T>G
|
XP_011531067.1:p.Phe208Val
|
|
|
XM_017003803.2:c.1273T>G
|
XP_016859292.1:p.Phe425Val
|
|
|
XR_001738703.2:n.1357T>G
|
|
|
|
NM_000821.7:c.1444T>G
MANE Select
|
NP_000812.2:p.Phe482Val
|
|
|
NM_001142269.4:c.1273T>G
|
NP_001135741.1:p.Phe425Val
|
|
