ENST00000378106.10:c.541G>T
MANE Select
|
ENSP00000367346.5:p.Asp181Tyr
|
|
ENST00000378081.9:c.541G>T
|
ENSP00000437325.1:p.Asp181Tyr
|
|
ENST00000378106.9:c.541G>T
|
ENSP00000367346.5:p.Asp181Tyr
|
|
ENST00000463598.1:c.457G>T
|
ENSP00000420497.1:p.Asp153Tyr
|
|
ENST00000464269.5:n.214G>T
|
|
|
ENST00000475968.5:n.418G>T
|
|
|
ENST00000476536.5:n.501G>T
|
|
|
ENST00000477732.5:n.502+3007G>T
|
|
|
ENST00000479716.5:n.62G>T
|
|
|
ENST00000481249.5:n.418G>T
|
|
|
ENST00000485738.5:n.519-1G>T
|
|
|
NM_001039375.2:c.457G>T
|
NP_001034464.1:p.Asp153Tyr
|
|
NM_024120.4:c.541G>T
|
NP_077025.2:p.Asp181Tyr
|
|
NR_029377.1:n.584G>T
|
|
|
XM_006723620.2:c.541G>T
|
XP_006723683.1:p.Asp181Tyr
|
|
XM_006723622.2:c.70G>T
|
XP_006723685.1:p.Asp24Tyr
|
|
XM_006723623.1:c.70G>T
|
XP_006723686.1:p.Asp24Tyr
|
|
XM_006723624.1:c.70G>T
|
XP_006723687.1:p.Asp24Tyr
|
|
XM_011529341.1:c.541G>T
|
XP_011527643.1:p.Asp181Tyr
|
|
XM_011529342.1:c.541G>T
|
XP_011527644.1:p.Asp181Tyr
|
|
XM_011529343.1:c.541G>T
|
XP_011527645.1:p.Asp181Tyr
|
|
XM_011529344.1:c.172G>T
|
XP_011527646.1:p.Asp58Tyr
|
|
XR_430269.2:n.561G>T
|
|
|
XR_937140.1:n.561G>T
|
|
|
NM_001352403.1:c.70G>T
|
NP_001339332.1:p.Asp24Tyr
|
|
NM_001352406.1:c.-21G>T
|
NP_001339335.1:n.-21G>T
|
|
NM_001352407.1:c.-21G>T
|
NP_001339336.1:n.-21G>T
|
|
NM_001352408.1:c.541G>T
|
NP_001339337.1:p.Asp181Tyr
|
|
NR_147978.1:n.584G>T
|
|
|
NR_147979.1:n.604G>T
|
|
|
NR_147980.1:n.480G>T
|
|
|
NR_147981.1:n.718G>T
|
|
|
NR_147982.1:n.718G>T
|
|
|
NR_147983.1:n.634G>T
|
|
|
XM_006723624.2:c.70G>T
|
XP_006723687.1:p.Asp24Tyr
|
|
XM_011529342.2:c.541G>T
|
XP_011527644.1:p.Asp181Tyr
|
|
XM_024451999.1:c.70G>T
|
XP_024307767.1:p.Asp24Tyr
|
|
XR_001754396.1:n.500G>T
|
|
|
XR_430269.3:n.561G>T
|
|
|
XR_937140.2:n.561G>T
|
|
|
NM_024120.5:c.541G>T
MANE Select
|
NP_077025.2:p.Asp181Tyr
|
|
NM_001039375.3:c.457G>T
|
NP_001034464.1:p.Asp153Tyr
|
|
NM_001352403.2:c.70G>T
|
NP_001339332.1:p.Asp24Tyr
|
|
NM_001352406.2:c.-21G>T
|
NP_001339335.1:n.-21G>T
|
|
NM_001352407.2:c.-21G>T
|
NP_001339336.1:n.-21G>T
|
|
NR_029377.2:n.582G>T
|
|
|
NR_147978.2:n.582G>T
|
|
|
NR_147979.2:n.602G>T
|
|
|
NR_147980.2:n.478G>T
|
|
|
NR_147981.2:n.716G>T
|
|
|
NR_147982.2:n.716G>T
|
|
|
NR_147983.2:n.632G>T
|
|
|
NM_001352408.2:c.541G>T
|
NP_001339337.1:p.Asp181Tyr
|
|