ENST00000361682.11:c.*10_*11insA
(COMT)
MANE Select
|
ENSP00000354511.6:n.*10_*11insA
|
|
ENST00000428707.2:c.*1319_*1320insA
(COMT)
|
ENSP00000387695.2:n.*1319_*1320insA
|
|
ENST00000676678.1:c.*10_*11insA
(COMT)
|
ENSP00000503719.1:n.*10_*11insA
|
|
ENST00000677397.1:c.*405_*406insA
(COMT)
|
ENSP00000503422.1:n.*405_*406insA
|
|
ENST00000677470.1:n.676_677insA
(COMT)
|
|
|
ENST00000677564.1:n.609_610insA
(COMT)
|
|
|
ENST00000677675.1:n.626_627insA
(COMT)
|
|
|
ENST00000678255.1:c.*10_*11insA
(COMT)
|
ENSP00000504402.1:n.*10_*11insA
|
|
ENST00000678769.1:c.*10_*11insA
(COMT)
|
ENSP00000503289.1:n.*10_*11insA
|
|
ENST00000678868.1:c.*10_*11insA
(COMT)
|
ENSP00000503583.1:n.*10_*11insA
|
|
ENST00000678945.1:n.694_695insA
(COMT)
|
|
|
ENST00000207636.9:c.*284_*285insA
(COMT)
|
ENSP00000207636.5:n.*284_*285insA
|
|
ENST00000361682.10:c.*10_*11insA
(COMT)
|
ENSP00000354511.6:n.*10_*11insA
|
|
ENST00000403710.5:c.*10_*11insA
(COMT)
|
ENSP00000385917.1:n.*10_*11insA
|
|
ENST00000406520.7:c.*10_*11insA
(COMT)
|
ENSP00000385150.3:n.*10_*11insA
|
|
ENST00000407537.5:c.*10_*11insA
(COMT)
|
ENSP00000384654.2:n.*10_*11insA
|
|
ENST00000449653.5:c.*10_*11insA
(COMT)
|
ENSP00000416778.1:n.*10_*11insA
|
|
NM_000754.3:c.*10_*11insA
(COMT)
|
NP_000745.1:n.*10_*11insA
|
|
NM_001135161.1:c.*10_*11insA
(COMT)
|
NP_001128633.1:n.*10_*11insA
|
|
NM_001135162.1:c.*10_*11insA
(COMT)
|
NP_001128634.1:n.*10_*11insA
|
|
NM_007310.2:c.*10_*11insA
(COMT)
|
NP_009294.1:n.*10_*11insA
|
|
XM_005261242.1:c.2764-1538_2764-1537insT
(ARVCF)
|
XP_005261299.1:n.2764-1538_2764-1537insT
|
|
XM_006724243.1:c.2782-1538_2782-1537insT
(ARVCF)
|
XP_006724306.1:n.2782-1538_2782-1537insT
|
|
XM_006724246.2:c.2536-1538_2536-1537insT
(ARVCF)
|
XP_006724309.1:n.2536-1538_2536-1537insT
|
|
XM_011529886.1:c.*10_*11insA
(COMT)
|
XP_011528188.1:n.*10_*11insA
|
|
XM_011530179.1:c.2749-1538_2749-1537insT
(ARVCF)
|
XP_011528481.1:n.2749-1538_2749-1537insT
|
|
XM_011530182.1:c.1348-1538_1348-1537insT
(ARVCF)
|
XP_011528484.1:n.1348-1538_1348-1537insT
|
|
NM_001362828.1:c.*10_*11insA
(COMT)
|
NP_001349757.1:n.*10_*11insA
|
|
XM_005261242.3:c.2764-1538_2764-1537insT
(ARVCF)
|
XP_005261299.1:n.2764-1538_2764-1537insT
|
|
XM_006724243.3:c.2782-1538_2782-1537insT
(ARVCF)
|
XP_006724306.1:n.2782-1538_2782-1537insT
|
|
XM_006724246.4:c.2536-1538_2536-1537insT
(ARVCF)
|
XP_006724309.1:n.2536-1538_2536-1537insT
|
|
XM_011529886.2:c.*10_*11insA
(COMT)
|
XP_011528188.2:n.*10_*11insA
|
|
XM_011530179.3:c.2749-1538_2749-1537insT
(ARVCF)
|
XP_011528481.1:n.2749-1538_2749-1537insT
|
|
XM_011530182.3:c.1348-1538_1348-1537insT
(ARVCF)
|
XP_011528484.1:n.1348-1538_1348-1537insT
|
|
XM_017028595.1:c.*10_*11insA
(COMT)
|
XP_016884084.1:n.*10_*11insA
|
|
XM_024452249.1:c.2536-1538_2536-1537insT
(ARVCF)
|
XP_024308017.1:n.2536-1538_2536-1537insT
|
|
NM_000754.4:c.*10_*11insA
(COMT)
MANE Select
|
NP_000745.1:n.*10_*11insA
|
|
NM_001135161.2:c.*10_*11insA
(COMT)
|
NP_001128633.1:n.*10_*11insA
|
|
NM_001135162.2:c.*10_*11insA
(COMT)
|
NP_001128634.1:n.*10_*11insA
|
|
NM_001362828.2:c.*10_*11insA
(COMT)
|
NP_001349757.1:n.*10_*11insA
|
|
NM_007310.3:c.*10_*11insA
(COMT)
|
NP_009294.1:n.*10_*11insA
|
|