|
ENST00000473665.2:n.5225T>A
|
|
|
|
ENST00000482662.2:n.3632T>A
|
|
|
|
ENST00000685865.1:n.1584T>A
|
|
|
|
ENST00000687250.1:n.1284T>A
|
|
|
|
ENST00000687995.1:n.1533T>A
|
|
|
|
ENST00000688205.1:c.*774T>A
|
ENSP00000509673.1:n.*774T>A
|
|
|
ENST00000688788.1:n.1420T>A
|
|
|
|
ENST00000689276.1:c.1112T>A
|
ENSP00000510012.1:p.Leu371Gln
|
|
|
ENST00000689576.1:c.1181T>A
|
ENSP00000508712.1:p.Leu394Gln
|
|
|
ENST00000690108.1:c.*837T>A
|
ENSP00000510617.1:n.*837T>A
|
|
|
ENST00000690468.1:c.902T>A
|
ENSP00000509078.1:p.Leu301Gln
|
|
|
ENST00000690595.1:c.506T>A
|
ENSP00000508979.1:p.Leu169Gln
|
|
|
ENST00000691348.1:c.1010T>A
|
ENSP00000509369.1:p.Leu337Gln
|
|
|
ENST00000691410.1:c.*758T>A
|
ENSP00000508479.1:n.*758T>A
|
|
|
ENST00000693287.1:c.497T>A
|
ENSP00000510264.1:p.Leu166Gln
|
|
|
ENST00000693681.1:c.494T>A
|
ENSP00000510789.1:p.Leu165Gln
|
|
|
ENST00000233838.9:c.1181T>A
MANE Select
|
ENSP00000233838.3:p.Leu394Gln
|
|
|
ENST00000233838.8:c.1181T>A
|
ENSP00000233838.3:p.Leu394Gln
|
|
|
ENST00000430215.7:c.1010T>A
|
ENSP00000408045.3:p.Leu337Gln
|
|
|
ENST00000465637.5:n.179-5041T>A
|
|
|
|
ENST00000473665.1:n.674T>A
|
|
|
|
ENST00000482662.1:n.598T>A
|
|
|
|
NM_000821.5:c.1181T>A
|
NP_000812.2:p.Leu394Gln
|
|
|
NM_000821.6:c.1181T>A
|
NP_000812.2:p.Leu394Gln
|
|
|
NM_001142269.2:c.1010T>A
|
NP_001135741.1:p.Leu337Gln
|
|
|
NM_001142269.3:c.1010T>A
|
NP_001135741.1:p.Leu337Gln
|
|
|
XM_005264259.3:c.1181T>A
|
XP_005264316.1:p.Leu394Gln
|
|
|
XM_011532764.1:c.359T>A
|
XP_011531066.1:p.Leu120Gln
|
|
|
XM_011532765.1:c.359T>A
|
XP_011531067.1:p.Leu120Gln
|
|
|
XR_939677.1:n.1246T>A
|
|
|
|
XM_005264259.5:c.1181T>A
|
XP_005264316.1:p.Leu394Gln
|
|
|
XM_011532764.3:c.359T>A
|
XP_011531066.1:p.Leu120Gln
|
|
|
XM_011532765.3:c.359T>A
|
XP_011531067.1:p.Leu120Gln
|
|
|
XM_017003803.2:c.1010T>A
|
XP_016859292.1:p.Leu337Gln
|
|
|
XR_001738703.2:n.1246T>A
|
|
|
|
NM_000821.7:c.1181T>A
MANE Select
|
NP_000812.2:p.Leu394Gln
|
|
|
NM_001142269.4:c.1010T>A
|
NP_001135741.1:p.Leu337Gln
|
|
