ENST00000361682.11:c.480C>T
(COMT)
MANE Select
|
ENSP00000354511.6:p.Asp160=
|
|
ENST00000428707.2:c.480C>T
(COMT)
|
ENSP00000387695.2:p.Asp160=
|
|
ENST00000676678.1:c.480C>T
(COMT)
|
ENSP00000503719.1:p.Asp160=
|
|
ENST00000677397.1:c.330C>T
(COMT)
|
ENSP00000503422.1:p.Asp110=
|
|
ENST00000677564.1:n.263C>T
(COMT)
|
|
|
ENST00000677675.1:n.280C>T
(COMT)
|
|
|
ENST00000678240.1:n.328C>T
(COMT)
|
|
|
ENST00000678255.1:c.480C>T
(COMT)
|
ENSP00000504402.1:p.Asp160=
|
|
ENST00000678769.1:c.480C>T
(COMT)
|
ENSP00000503289.1:p.Asp160=
|
|
ENST00000678868.1:c.480C>T
(COMT)
|
ENSP00000503583.1:p.Asp160=
|
|
ENST00000678945.1:n.290C>T
(COMT)
|
|
|
ENST00000207636.9:c.480C>T
(COMT)
|
ENSP00000207636.5:p.Asp160=
|
|
ENST00000361682.10:c.480C>T
(COMT)
|
ENSP00000354511.6:p.Asp160=
|
|
ENST00000403184.5:c.480C>T
(COMT)
|
ENSP00000383966.1:p.Asp160=
|
|
ENST00000403710.5:c.480C>T
(COMT)
|
ENSP00000385917.1:p.Asp160=
|
|
ENST00000406520.7:c.480C>T
(COMT)
|
ENSP00000385150.3:p.Asp160=
|
|
ENST00000407537.5:c.480C>T
(COMT)
|
ENSP00000384654.2:p.Asp160=
|
|
ENST00000412786.5:c.480C>T
(COMT)
|
ENSP00000403958.1:p.Asp160=
|
|
ENST00000428707.1:c.58C>T
(COMT)
|
|
|
ENST00000449653.5:c.330C>T
(COMT)
|
ENSP00000416778.1:p.Asp110=
|
|
ENST00000493893.1:n.218C>T
(COMT)
|
|
|
NM_000754.3:c.480C>T
(COMT)
|
NP_000745.1:p.Asp160=
|
|
NM_001135161.1:c.480C>T
(COMT)
|
NP_001128633.1:p.Asp160=
|
|
NM_001135162.1:c.480C>T
(COMT)
|
NP_001128634.1:p.Asp160=
|
|
NM_007310.2:c.330C>T
(COMT)
|
NP_009294.1:p.Asp110=
|
|
NR_039918.1:n.4C>T
(MIR4761)
|
|
|
XM_011529885.1:c.594C>T
(COMT)
|
XP_011528187.1:p.Asp198=
|
|
XM_011529886.1:c.594C>T
(COMT)
|
XP_011528188.1:p.Asp198=
|
|
XM_011529887.1:c.480C>T
(COMT)
|
XP_011528189.1:p.Asp160=
|
|
XM_011529888.1:c.480C>T
(COMT)
|
XP_011528190.1:p.Asp160=
|
|
XM_011529889.1:c.480C>T
(COMT)
|
XP_011528191.1:p.Asp160=
|
|
XM_011529890.1:c.480C>T
(COMT)
|
XP_011528192.1:p.Asp160=
|
|
XM_011529891.1:c.480C>T
(COMT)
|
XP_011528193.1:p.Asp160=
|
|
NM_001362828.1:c.480C>T
(COMT)
|
NP_001349757.1:p.Asp160=
|
|
XM_011529886.2:c.891C>T
(COMT)
|
XP_011528188.2:p.Asp297=
|
|
XM_017028595.1:c.480C>T
(COMT)
|
XP_016884084.1:p.Asp160=
|
|
NM_000754.4:c.480C>T
(COMT)
MANE Select
|
NP_000745.1:p.Asp160=
|
|
NM_001135161.2:c.480C>T
(COMT)
|
NP_001128633.1:p.Asp160=
|
|
NM_001135162.2:c.480C>T
(COMT)
|
NP_001128634.1:p.Asp160=
|
|
NM_001362828.2:c.480C>T
(COMT)
|
NP_001349757.1:p.Asp160=
|
|
NM_007310.3:c.330C>T
(COMT)
|
NP_009294.1:p.Asp110=
|
|