|
ENST00000473665.2:n.6066G>T
|
|
|
|
ENST00000482662.2:n.4473G>T
|
|
|
|
ENST00000685865.1:n.2425G>T
|
|
|
|
ENST00000687250.1:n.2125G>T
|
|
|
|
ENST00000687995.1:n.1940G>T
|
|
|
|
ENST00000688205.1:c.*1181G>T
|
ENSP00000509673.1:n.*1181G>T
|
|
|
ENST00000688788.1:n.1827G>T
|
|
|
|
ENST00000689276.1:c.1519G>T
|
ENSP00000510012.1:p.Val507Phe
|
|
|
ENST00000689576.1:c.*207G>T
|
ENSP00000508712.1:n.*207G>T
|
|
|
ENST00000690108.1:c.*1244G>T
|
ENSP00000510617.1:n.*1244G>T
|
|
|
ENST00000690468.1:c.*140G>T
|
ENSP00000509078.1:n.*140G>T
|
|
|
ENST00000690595.1:c.913G>T
|
ENSP00000508979.1:p.Val305Phe
|
|
|
ENST00000691348.1:c.*140G>T
|
ENSP00000509369.1:n.*140G>T
|
|
|
ENST00000691410.1:c.*1165G>T
|
ENSP00000508479.1:n.*1165G>T
|
|
|
ENST00000693287.1:c.904G>T
|
ENSP00000510264.1:p.Val302Phe
|
|
|
ENST00000693681.1:c.901G>T
|
ENSP00000510789.1:p.Val301Phe
|
|
|
ENST00000233838.9:c.1588G>T
MANE Select
|
ENSP00000233838.3:p.Val530Phe
|
|
|
ENST00000233838.8:c.1588G>T
|
ENSP00000233838.3:p.Val530Phe
|
|
|
ENST00000430215.7:c.1417G>T
|
ENSP00000408045.3:p.Val473Phe
|
|
|
ENST00000465637.5:n.179-3829G>T
|
|
|
|
NM_000821.5:c.1588G>T
|
NP_000812.2:p.Val530Phe
|
|
|
NM_000821.6:c.1588G>T
|
NP_000812.2:p.Val530Phe
|
|
|
NM_001142269.2:c.1417G>T
|
NP_001135741.1:p.Val473Phe
|
|
|
NM_001142269.3:c.1417G>T
|
NP_001135741.1:p.Val473Phe
|
|
|
XM_005264259.3:c.1588G>T
|
XP_005264316.1:p.Val530Phe
|
|
|
XM_011532764.1:c.766G>T
|
XP_011531066.1:p.Val256Phe
|
|
|
XM_011532765.1:c.766G>T
|
XP_011531067.1:p.Val256Phe
|
|
|
XR_939677.1:n.1501G>T
|
|
|
|
XM_005264259.5:c.1588G>T
|
XP_005264316.1:p.Val530Phe
|
|
|
XM_011532764.3:c.766G>T
|
XP_011531066.1:p.Val256Phe
|
|
|
XM_011532765.3:c.766G>T
|
XP_011531067.1:p.Val256Phe
|
|
|
XM_017003803.2:c.1417G>T
|
XP_016859292.1:p.Val473Phe
|
|
|
XR_001738703.2:n.1501G>T
|
|
|
|
NM_000821.7:c.1588G>T
MANE Select
|
NP_000812.2:p.Val530Phe
|
|
|
NM_001142269.4:c.1417G>T
|
NP_001135741.1:p.Val473Phe
|
|
