ENST00000378106.10:c.623G>C
MANE Select
|
ENSP00000367346.5:p.Arg208Thr
|
|
ENST00000378081.9:c.623G>C
|
ENSP00000437325.1:p.Arg208Thr
|
|
ENST00000378106.9:c.623G>C
|
ENSP00000367346.5:p.Arg208Thr
|
|
ENST00000463598.1:c.539G>C
|
ENSP00000420497.1:p.Arg180Thr
|
|
ENST00000464269.5:n.296G>C
|
|
|
ENST00000475968.5:n.500G>C
|
|
|
ENST00000476124.1:n.22G>C
|
|
|
ENST00000476536.5:n.583G>C
|
|
|
ENST00000477732.5:n.502+3089G>C
|
|
|
ENST00000479716.5:n.144G>C
|
|
|
ENST00000481249.5:n.500G>C
|
|
|
ENST00000485738.5:n.600G>C
|
|
|
ENST00000487478.5:n.47G>C
|
|
|
NM_001039375.2:c.539G>C
|
NP_001034464.1:p.Arg180Thr
|
|
NM_024120.4:c.623G>C
|
NP_077025.2:p.Arg208Thr
|
|
NR_029377.1:n.666G>C
|
|
|
XM_006723620.2:c.623G>C
|
XP_006723683.1:p.Arg208Thr
|
|
XM_006723622.2:c.152G>C
|
XP_006723685.1:p.Arg51Thr
|
|
XM_006723623.1:c.152G>C
|
XP_006723686.1:p.Arg51Thr
|
|
XM_006723624.1:c.152G>C
|
XP_006723687.1:p.Arg51Thr
|
|
XM_011529341.1:c.623G>C
|
XP_011527643.1:p.Arg208Thr
|
|
XM_011529342.1:c.623G>C
|
XP_011527644.1:p.Arg208Thr
|
|
XM_011529343.1:c.623G>C
|
XP_011527645.1:p.Arg208Thr
|
|
XM_011529344.1:c.254G>C
|
XP_011527646.1:p.Arg85Thr
|
|
XR_430269.2:n.643G>C
|
|
|
XR_937140.1:n.643G>C
|
|
|
NM_001352403.1:c.152G>C
|
NP_001339332.1:p.Arg51Thr
|
|
NM_001352406.1:c.62G>C
|
NP_001339335.1:p.Arg21Thr
|
|
NM_001352407.1:c.62G>C
|
NP_001339336.1:p.Arg21Thr
|
|
NM_001352408.1:c.623G>C
|
NP_001339337.1:p.Arg208Thr
|
|
NR_147978.1:n.666G>C
|
|
|
NR_147979.1:n.686G>C
|
|
|
NR_147980.1:n.562G>C
|
|
|
NR_147981.1:n.800G>C
|
|
|
NR_147982.1:n.800G>C
|
|
|
NR_147983.1:n.716G>C
|
|
|
XM_006723624.2:c.152G>C
|
XP_006723687.1:p.Arg51Thr
|
|
XM_011529342.2:c.623G>C
|
XP_011527644.1:p.Arg208Thr
|
|
XM_024451999.1:c.152G>C
|
XP_024307767.1:p.Arg51Thr
|
|
XR_001754396.1:n.582G>C
|
|
|
XR_430269.3:n.643G>C
|
|
|
XR_937140.2:n.643G>C
|
|
|
NM_024120.5:c.623G>C
MANE Select
|
NP_077025.2:p.Arg208Thr
|
|
NM_001039375.3:c.539G>C
|
NP_001034464.1:p.Arg180Thr
|
|
NM_001352403.2:c.152G>C
|
NP_001339332.1:p.Arg51Thr
|
|
NM_001352406.2:c.62G>C
|
NP_001339335.1:p.Arg21Thr
|
|
NM_001352407.2:c.62G>C
|
NP_001339336.1:p.Arg21Thr
|
|
NR_029377.2:n.664G>C
|
|
|
NR_147978.2:n.664G>C
|
|
|
NR_147979.2:n.684G>C
|
|
|
NR_147980.2:n.560G>C
|
|
|
NR_147981.2:n.798G>C
|
|
|
NR_147982.2:n.798G>C
|
|
|
NR_147983.2:n.714G>C
|
|
|
NM_001352408.2:c.623G>C
|
NP_001339337.1:p.Arg208Thr
|
|