|
ENST00000473665.2:n.5991C>T
|
|
|
|
ENST00000482662.2:n.4398C>T
|
|
|
|
ENST00000685865.1:n.2350C>T
|
|
|
|
ENST00000687250.1:n.2050C>T
|
|
|
|
ENST00000687995.1:n.1865C>T
|
|
|
|
ENST00000688205.1:c.*1106C>T
|
ENSP00000509673.1:n.*1106C>T
|
|
|
ENST00000688788.1:n.1752C>T
|
|
|
|
ENST00000689276.1:c.1444C>T
|
ENSP00000510012.1:p.Leu482Phe
|
|
|
ENST00000689576.1:c.*132C>T
|
ENSP00000508712.1:n.*132C>T
|
|
|
ENST00000690108.1:c.*1169C>T
|
ENSP00000510617.1:n.*1169C>T
|
|
|
ENST00000690468.1:c.*65C>T
|
ENSP00000509078.1:n.*65C>T
|
|
|
ENST00000690595.1:c.838C>T
|
ENSP00000508979.1:p.Leu280Phe
|
|
|
ENST00000691348.1:c.*65C>T
|
ENSP00000509369.1:n.*65C>T
|
|
|
ENST00000691410.1:c.*1090C>T
|
ENSP00000508479.1:n.*1090C>T
|
|
|
ENST00000693287.1:c.829C>T
|
ENSP00000510264.1:p.Leu277Phe
|
|
|
ENST00000693681.1:c.826C>T
|
ENSP00000510789.1:p.Leu276Phe
|
|
|
ENST00000233838.9:c.1513C>T
MANE Select
|
ENSP00000233838.3:p.Leu505Phe
|
|
|
ENST00000233838.8:c.1513C>T
|
ENSP00000233838.3:p.Leu505Phe
|
|
|
ENST00000430215.7:c.1342C>T
|
ENSP00000408045.3:p.Leu448Phe
|
|
|
ENST00000465637.5:n.179-3904C>T
|
|
|
|
NM_000821.5:c.1513C>T
|
NP_000812.2:p.Leu505Phe
|
|
|
NM_000821.6:c.1513C>T
|
NP_000812.2:p.Leu505Phe
|
|
|
NM_001142269.2:c.1342C>T
|
NP_001135741.1:p.Leu448Phe
|
|
|
NM_001142269.3:c.1342C>T
|
NP_001135741.1:p.Leu448Phe
|
|
|
XM_005264259.3:c.1513C>T
|
XP_005264316.1:p.Leu505Phe
|
|
|
XM_011532764.1:c.691C>T
|
XP_011531066.1:p.Leu231Phe
|
|
|
XM_011532765.1:c.691C>T
|
XP_011531067.1:p.Leu231Phe
|
|
|
XR_939677.1:n.1426C>T
|
|
|
|
XM_005264259.5:c.1513C>T
|
XP_005264316.1:p.Leu505Phe
|
|
|
XM_011532764.3:c.691C>T
|
XP_011531066.1:p.Leu231Phe
|
|
|
XM_011532765.3:c.691C>T
|
XP_011531067.1:p.Leu231Phe
|
|
|
XM_017003803.2:c.1342C>T
|
XP_016859292.1:p.Leu448Phe
|
|
|
XR_001738703.2:n.1426C>T
|
|
|
|
NM_000821.7:c.1513C>T
MANE Select
|
NP_000812.2:p.Leu505Phe
|
|
|
NM_001142269.4:c.1342C>T
|
NP_001135741.1:p.Leu448Phe
|
|
