|
ENST00000473665.2:n.5956G>T
|
|
|
|
ENST00000482662.2:n.4363G>T
|
|
|
|
ENST00000685865.1:n.2315G>T
|
|
|
|
ENST00000687250.1:n.2015G>T
|
|
|
|
ENST00000687995.1:n.1830G>T
|
|
|
|
ENST00000688205.1:c.*1071G>T
|
ENSP00000509673.1:n.*1071G>T
|
|
|
ENST00000688788.1:n.1717G>T
|
|
|
|
ENST00000689276.1:c.1409G>T
|
ENSP00000510012.1:p.Trp470Leu
|
|
|
ENST00000689576.1:c.*97G>T
|
ENSP00000508712.1:n.*97G>T
|
|
|
ENST00000690108.1:c.*1134G>T
|
ENSP00000510617.1:n.*1134G>T
|
|
|
ENST00000690468.1:c.*30G>T
|
ENSP00000509078.1:n.*30G>T
|
|
|
ENST00000690595.1:c.803G>T
|
ENSP00000508979.1:p.Trp268Leu
|
|
|
ENST00000691348.1:c.*30G>T
|
ENSP00000509369.1:n.*30G>T
|
|
|
ENST00000691410.1:c.*1055G>T
|
ENSP00000508479.1:n.*1055G>T
|
|
|
ENST00000693287.1:c.794G>T
|
ENSP00000510264.1:p.Trp265Leu
|
|
|
ENST00000693681.1:c.791G>T
|
ENSP00000510789.1:p.Trp264Leu
|
|
|
ENST00000233838.9:c.1478G>T
MANE Select
|
ENSP00000233838.3:p.Trp493Leu
|
|
|
ENST00000233838.8:c.1478G>T
|
ENSP00000233838.3:p.Trp493Leu
|
|
|
ENST00000430215.7:c.1307G>T
|
ENSP00000408045.3:p.Trp436Leu
|
|
|
ENST00000465637.5:n.179-3939G>T
|
|
|
|
NM_000821.5:c.1478G>T
|
NP_000812.2:p.Trp493Leu
|
|
|
NM_000821.6:c.1478G>T
|
NP_000812.2:p.Trp493Leu
|
|
|
NM_001142269.2:c.1307G>T
|
NP_001135741.1:p.Trp436Leu
|
|
|
NM_001142269.3:c.1307G>T
|
NP_001135741.1:p.Trp436Leu
|
|
|
XM_005264259.3:c.1478G>T
|
XP_005264316.1:p.Trp493Leu
|
|
|
XM_011532764.1:c.656G>T
|
XP_011531066.1:p.Trp219Leu
|
|
|
XM_011532765.1:c.656G>T
|
XP_011531067.1:p.Trp219Leu
|
|
|
XR_939677.1:n.1391G>T
|
|
|
|
XM_005264259.5:c.1478G>T
|
XP_005264316.1:p.Trp493Leu
|
|
|
XM_011532764.3:c.656G>T
|
XP_011531066.1:p.Trp219Leu
|
|
|
XM_011532765.3:c.656G>T
|
XP_011531067.1:p.Trp219Leu
|
|
|
XM_017003803.2:c.1307G>T
|
XP_016859292.1:p.Trp436Leu
|
|
|
XR_001738703.2:n.1391G>T
|
|
|
|
NM_000821.7:c.1478G>T
MANE Select
|
NP_000812.2:p.Trp493Leu
|
|
|
NM_001142269.4:c.1307G>T
|
NP_001135741.1:p.Trp436Leu
|
|
