|
ENST00000473665.2:n.5192T>A
|
|
|
|
ENST00000482662.2:n.3599T>A
|
|
|
|
ENST00000685865.1:n.1551T>A
|
|
|
|
ENST00000687250.1:n.1251T>A
|
|
|
|
ENST00000687995.1:n.1500T>A
|
|
|
|
ENST00000688205.1:c.*741T>A
|
ENSP00000509673.1:n.*741T>A
|
|
|
ENST00000688788.1:n.1387T>A
|
|
|
|
ENST00000689276.1:c.1079T>A
|
ENSP00000510012.1:p.Leu360His
|
|
|
ENST00000689576.1:c.1148T>A
|
ENSP00000508712.1:p.Leu383His
|
|
|
ENST00000690108.1:c.*804T>A
|
ENSP00000510617.1:n.*804T>A
|
|
|
ENST00000690468.1:c.869T>A
|
ENSP00000509078.1:p.Leu290His
|
|
|
ENST00000690595.1:c.473T>A
|
ENSP00000508979.1:p.Leu158His
|
|
|
ENST00000691348.1:c.977T>A
|
ENSP00000509369.1:p.Leu326His
|
|
|
ENST00000691410.1:c.*725T>A
|
ENSP00000508479.1:n.*725T>A
|
|
|
ENST00000693287.1:c.464T>A
|
ENSP00000510264.1:p.Leu155His
|
|
|
ENST00000693681.1:c.461T>A
|
ENSP00000510789.1:p.Leu154His
|
|
|
ENST00000233838.9:c.1148T>A
MANE Select
|
ENSP00000233838.3:p.Leu383His
|
|
|
ENST00000233838.8:c.1148T>A
|
ENSP00000233838.3:p.Leu383His
|
|
|
ENST00000430215.7:c.977T>A
|
ENSP00000408045.3:p.Leu326His
|
|
|
ENST00000465637.5:n.179-5235T>A
|
|
|
|
ENST00000473665.1:n.641T>A
|
|
|
|
ENST00000482662.1:n.565T>A
|
|
|
|
NM_000821.5:c.1148T>A
|
NP_000812.2:p.Leu383His
|
|
|
NM_000821.6:c.1148T>A
|
NP_000812.2:p.Leu383His
|
|
|
NM_001142269.2:c.977T>A
|
NP_001135741.1:p.Leu326His
|
|
|
NM_001142269.3:c.977T>A
|
NP_001135741.1:p.Leu326His
|
|
|
XM_005264259.3:c.1148T>A
|
XP_005264316.1:p.Leu383His
|
|
|
XM_011532764.1:c.326T>A
|
XP_011531066.1:p.Leu109His
|
|
|
XM_011532765.1:c.326T>A
|
XP_011531067.1:p.Leu109His
|
|
|
XR_939677.1:n.1213T>A
|
|
|
|
XM_005264259.5:c.1148T>A
|
XP_005264316.1:p.Leu383His
|
|
|
XM_011532764.3:c.326T>A
|
XP_011531066.1:p.Leu109His
|
|
|
XM_011532765.3:c.326T>A
|
XP_011531067.1:p.Leu109His
|
|
|
XM_017003803.2:c.977T>A
|
XP_016859292.1:p.Leu326His
|
|
|
XR_001738703.2:n.1213T>A
|
|
|
|
NM_000821.7:c.1148T>A
MANE Select
|
NP_000812.2:p.Leu383His
|
|
|
NM_001142269.4:c.977T>A
|
NP_001135741.1:p.Leu326His
|
|
