|
ENST00000373560.7:c.438-16244T>G
|
ENSP00000362661.2:n.438-16244T>G
|
|
|
ENST00000373568.7:c.584T>G
|
ENSP00000362669.3:p.Val195Gly
|
|
|
ENST00000373571.6:c.584T>G
|
ENSP00000362672.1:p.Val195Gly
|
|
|
ENST00000373573.9:c.584T>G
MANE Select
|
ENSP00000362674.3:p.Val195Gly
|
|
|
ENST00000373583.6:c.551-1932T>G
|
ENSP00000362685.2:n.551-1932T>G
|
|
|
ENST00000373589.9:c.311T>G
|
ENSP00000362691.4:p.Val104Gly
|
|
|
ENST00000412342.6:c.*282T>G
|
ENSP00000400180.1:n.*282T>G
|
|
|
ENST00000415409.6:c.584T>G
|
ENSP00000396424.2:p.Val195Gly
|
|
|
ENST00000436675.6:c.550+4183T>G
|
ENSP00000416489.1:n.550+4183T>G
|
|
|
ENST00000439122.7:c.584T>G
|
ENSP00000414486.2:p.Val195Gly
|
|
|
ENST00000478743.2:n.670T>G
|
|
|
|
ENST00000647594.1:c.584T>G
|
ENSP00000496814.1:p.Val195Gly
|
|
|
ENST00000647606.1:c.359T>G
|
|
|
|
ENST00000647613.1:c.*382-1932T>G
|
ENSP00000497911.1:n.*382-1932T>G
|
|
|
ENST00000647641.1:n.671T>G
|
|
|
|
ENST00000647654.1:c.311T>G
|
ENSP00000497568.1:p.Val104Gly
|
|
|
ENST00000647718.1:n.639T>G
|
|
|
|
ENST00000647859.1:c.584T>G
|
ENSP00000497530.1:p.Val195Gly
|
|
|
ENST00000647886.1:c.584T>G
|
ENSP00000497188.1:p.Val195Gly
|
|
|
ENST00000647974.1:c.328T>G
|
|
|
|
ENST00000647980.1:c.578T>G
|
ENSP00000498002.1:p.Val193Gly
|
|
|
ENST00000648036.1:c.578T>G
|
ENSP00000496994.1:p.Val193Gly
|
|
|
ENST00000648139.1:c.438-26242T>G
|
ENSP00000496818.1:n.438-26242T>G
|
|
|
ENST00000648285.1:n.367T>G
|
|
|
|
ENST00000648298.1:c.584T>G
|
ENSP00000496866.1:p.Val195Gly
|
|
|
ENST00000648452.1:c.584T>G
|
ENSP00000497268.1:p.Val195Gly
|
|
|
ENST00000648459.1:c.135-26242T>G
|
ENSP00000498072.1:n.135-26242T>G
|
|
|
ENST00000648504.1:c.521T>G
|
ENSP00000497668.1:p.Val174Gly
|
|
|
ENST00000648577.1:c.*188T>G
|
ENSP00000497552.1:n.*188T>G
|
|
|
ENST00000648711.1:c.209T>G
|
ENSP00000498040.1:p.Val70Gly
|
|
|
ENST00000648731.1:c.690T>G
|
|
|
|
ENST00000648834.1:c.584T>G
|
ENSP00000497764.1:p.Val195Gly
|
|
|
ENST00000648850.1:c.219T>G
|
|
|
|
ENST00000648855.1:n.508T>G
|
|
|
|
ENST00000648870.1:c.584T>G
|
ENSP00000497599.1:p.Val195Gly
|
|
|
ENST00000648922.1:c.584T>G
|
ENSP00000497072.1:p.Val195Gly
|
|
|
ENST00000648939.1:c.584T>G
|
ENSP00000497442.1:p.Val195Gly
|
|
|
ENST00000648962.1:c.550+4183T>G
|
ENSP00000497516.1:n.550+4183T>G
|
|
|
ENST00000649097.1:c.584T>G
|
ENSP00000497551.1:p.Val195Gly
|
|
|
ENST00000649116.1:c.*141T>G
|
ENSP00000497925.1:n.*141T>G
|
|
|
ENST00000649181.1:c.471T>G
|
ENSP00000498150.1:p.Ser157Arg
|
|
|
ENST00000649242.1:c.*188T>G
|
ENSP00000497943.1:n.*188T>G
|
|
|
ENST00000649274.1:c.522T>G
|
ENSP00000497032.1:n.522T>G
|
|
|
ENST00000649518.1:c.*188T>G
|
ENSP00000498169.1:n.*188T>G
|
|
|
ENST00000649543.1:c.*188T>G
|
ENSP00000496826.1:n.*188T>G
|
|
|
ENST00000649752.1:c.311T>G
|
ENSP00000497267.1:p.Val104Gly
|
|
|
ENST00000650076.1:c.58T>G
|
|
|
|
ENST00000650126.1:c.551-1932T>G
|
ENSP00000498144.1:n.551-1932T>G
|
|
|
ENST00000650471.1:c.*28T>G
|
ENSP00000498027.1:n.*28T>G
|
|
|
ENST00000650604.1:c.165-26242T>G
|
ENSP00000497105.1:n.165-26242T>G
|
|
|
ENST00000373559.8:c.278-1932T>G
|
ENSP00000362660.4:n.278-1932T>G
|
|
|
ENST00000373560.6:c.438-16244T>G
|
ENSP00000362661.2:n.438-16244T>G
|
|
|
ENST00000373568.6:c.311T>G
|
ENSP00000362669.2:p.Val104Gly
|
|
|
ENST00000373571.5:c.584T>G
|
ENSP00000362672.1:p.Val195Gly
|
|
|
ENST00000373573.7:c.584T>G
|
ENSP00000362674.3:p.Val195Gly
|
|
|
ENST00000373583.5:c.164+81084T>G
|
ENSP00000362685.1:n.164+81084T>G
|
|
|
ENST00000373589.8:c.311T>G
|
ENSP00000362691.4:p.Val104Gly
|
|
|
ENST00000412342.5:c.*282T>G
|
ENSP00000400180.1:n.*282T>G
|
|
|
ENST00000415409.5:c.551-1932T>G
|
ENSP00000396424.1:n.551-1932T>G
|
|
|
ENST00000436675.5:c.550+4183T>G
|
ENSP00000416489.1:n.550+4183T>G
|
|
|
ENST00000439122.6:c.584T>G
|
ENSP00000414486.2:p.Val195Gly
|
|
|
ENST00000478743.1:n.524T>G
|
|
|
|
NM_001166418.1:c.311T>G
|
NP_001159890.1:p.Val104Gly
|
|
|
NM_001166419.1:c.584T>G
|
NP_001159891.1:p.Val195Gly
|
|
|
NM_001166448.1:c.278-1932T>G
|
NP_001159920.1:n.278-1932T>G
|
|
|
NM_018486.2:c.584T>G
|
NP_060956.1:p.Val195Gly
|
|
|
NR_051952.1:n.784T>G
|
|
|
|
XM_011530986.1:c.584T>G
|
XP_011529288.1:p.Val195Gly
|
|
|
XM_011530987.1:c.584T>G
|
XP_011529289.1:p.Val195Gly
|
|
|
XM_011530988.1:c.584T>G
|
XP_011529290.1:p.Val195Gly
|
|
|
XR_938402.1:n.670T>G
|
|
|
|
XM_011530986.3:c.584T>G
|
XP_011529288.3:p.Val195Gly
|
|
|
XM_017029640.2:c.551-1932T>G
|
XP_016885129.2:n.551-1932T>G
|
|
|
XM_017029641.2:c.551-1932T>G
|
XP_016885130.2:n.551-1932T>G
|
|
|
XM_017029642.1:c.425T>G
|
XP_016885131.1:p.Val142Gly
|
|
|
XM_017029643.2:c.552-26242T>G
|
XP_016885132.1:n.552-26242T>G
|
|
|
XM_017029644.2:c.392-1932T>G
|
XP_016885133.1:n.392-1932T>G
|
|
|
XM_017029645.2:c.552-26242T>G
|
XP_016885134.1:n.552-26242T>G
|
|
|
XM_017029646.1:c.197T>G
|
XP_016885135.1:p.Val66Gly
|
|
|
XM_017029647.2:c.551-1932T>G
|
XP_016885136.2:n.551-1932T>G
|
|
|
XM_024452405.1:c.-2T>G
|
XP_024308173.1:n.-2T>G
|
|
|
XR_001755711.2:n.670T>G
|
|
|
|
XR_002958779.1:n.670T>G
|
|
|
|
XR_002958780.1:n.670T>G
|
|
|
|
XR_002958781.1:n.670T>G
|
|
|
|
XR_002958782.1:n.646T>G
|
|
|
|
XR_002958783.1:n.646T>G
|
|
|
|
XR_938402.3:n.670T>G
|
|
|
|
NM_018486.3:c.584T>G
MANE Select
|
NP_060956.1:p.Val195Gly
|
|
|
NM_001166418.2:c.311T>G
|
NP_001159890.1:p.Val104Gly
|
|
|
NM_001166419.2:c.584T>G
|
NP_001159891.1:p.Val195Gly
|
|
|
NM_001166448.2:c.278-1932T>G
|
NP_001159920.1:n.278-1932T>G
|
|
|
NR_051952.2:n.524T>G
|
|
|
