|
ENST00000473665.2:n.5190T>G
|
|
|
|
ENST00000482662.2:n.3597T>G
|
|
|
|
ENST00000685865.1:n.1549T>G
|
|
|
|
ENST00000687250.1:n.1249T>G
|
|
|
|
ENST00000687995.1:n.1498T>G
|
|
|
|
ENST00000688205.1:c.*739T>G
|
ENSP00000509673.1:n.*739T>G
|
|
|
ENST00000688788.1:n.1385T>G
|
|
|
|
ENST00000689276.1:c.1077T>G
|
ENSP00000510012.1:p.Phe359Leu
|
|
|
ENST00000689576.1:c.1146T>G
|
ENSP00000508712.1:p.Phe382Leu
|
|
|
ENST00000690108.1:c.*802T>G
|
ENSP00000510617.1:n.*802T>G
|
|
|
ENST00000690468.1:c.867T>G
|
ENSP00000509078.1:p.Phe289Leu
|
|
|
ENST00000690595.1:c.471T>G
|
ENSP00000508979.1:p.Phe157Leu
|
|
|
ENST00000691348.1:c.975T>G
|
ENSP00000509369.1:p.Phe325Leu
|
|
|
ENST00000691410.1:c.*723T>G
|
ENSP00000508479.1:n.*723T>G
|
|
|
ENST00000693287.1:c.462T>G
|
ENSP00000510264.1:p.Phe154Leu
|
|
|
ENST00000693681.1:c.459T>G
|
ENSP00000510789.1:p.Phe153Leu
|
|
|
ENST00000233838.9:c.1146T>G
MANE Select
|
ENSP00000233838.3:p.Phe382Leu
|
|
|
ENST00000233838.8:c.1146T>G
|
ENSP00000233838.3:p.Phe382Leu
|
|
|
ENST00000430215.7:c.975T>G
|
ENSP00000408045.3:p.Phe325Leu
|
|
|
ENST00000465637.5:n.179-5237T>G
|
|
|
|
ENST00000473665.1:n.639T>G
|
|
|
|
ENST00000482662.1:n.563T>G
|
|
|
|
NM_000821.5:c.1146T>G
|
NP_000812.2:p.Phe382Leu
|
|
|
NM_000821.6:c.1146T>G
|
NP_000812.2:p.Phe382Leu
|
|
|
NM_001142269.2:c.975T>G
|
NP_001135741.1:p.Phe325Leu
|
|
|
NM_001142269.3:c.975T>G
|
NP_001135741.1:p.Phe325Leu
|
|
|
XM_005264259.3:c.1146T>G
|
XP_005264316.1:p.Phe382Leu
|
|
|
XM_011532764.1:c.324T>G
|
XP_011531066.1:p.Phe108Leu
|
|
|
XM_011532765.1:c.324T>G
|
XP_011531067.1:p.Phe108Leu
|
|
|
XR_939677.1:n.1211T>G
|
|
|
|
XM_005264259.5:c.1146T>G
|
XP_005264316.1:p.Phe382Leu
|
|
|
XM_011532764.3:c.324T>G
|
XP_011531066.1:p.Phe108Leu
|
|
|
XM_011532765.3:c.324T>G
|
XP_011531067.1:p.Phe108Leu
|
|
|
XM_017003803.2:c.975T>G
|
XP_016859292.1:p.Phe325Leu
|
|
|
XR_001738703.2:n.1211T>G
|
|
|
|
NM_000821.7:c.1146T>G
MANE Select
|
NP_000812.2:p.Phe382Leu
|
|
|
NM_001142269.4:c.975T>G
|
NP_001135741.1:p.Phe325Leu
|
|
