ENST00000361682.11:c.*465G>T
(COMT)
MANE Select
|
ENSP00000354511.6:n.*465G>T
|
|
ENST00000677564.1:n.1064G>T
(COMT)
|
|
|
ENST00000678255.1:c.*465G>T
(COMT)
|
ENSP00000504402.1:n.*465G>T
|
|
ENST00000678769.1:c.*465G>T
(COMT)
|
ENSP00000503289.1:n.*465G>T
|
|
ENST00000678868.1:c.*465G>T
(COMT)
|
ENSP00000503583.1:n.*465G>T
|
|
ENST00000678945.1:n.1149G>T
(COMT)
|
|
|
ENST00000361682.10:c.*465G>T
(COMT)
|
ENSP00000354511.6:n.*465G>T
|
|
NM_000754.3:c.*465G>T
(COMT)
|
NP_000745.1:n.*465G>T
|
|
NM_001135161.1:c.*465G>T
(COMT)
|
NP_001128633.1:n.*465G>T
|
|
NM_001135162.1:c.*465G>T
(COMT)
|
NP_001128634.1:n.*465G>T
|
|
NM_007310.2:c.*465G>T
(COMT)
|
NP_009294.1:n.*465G>T
|
|
XM_005261242.1:c.2764-1992C>A
(ARVCF)
|
XP_005261299.1:n.2764-1992C>A
|
|
XM_006724243.1:c.2782-1992C>A
(ARVCF)
|
XP_006724306.1:n.2782-1992C>A
|
|
XM_006724246.2:c.2536-1992C>A
(ARVCF)
|
XP_006724309.1:n.2536-1992C>A
|
|
XM_011530179.1:c.2749-1992C>A
(ARVCF)
|
XP_011528481.1:n.2749-1992C>A
|
|
XM_011530182.1:c.1348-1992C>A
(ARVCF)
|
XP_011528484.1:n.1348-1992C>A
|
|
NM_001362828.1:c.*465G>T
(COMT)
|
NP_001349757.1:n.*465G>T
|
|
XM_005261242.3:c.2764-1992C>A
(ARVCF)
|
XP_005261299.1:n.2764-1992C>A
|
|
XM_006724243.3:c.2782-1992C>A
(ARVCF)
|
XP_006724306.1:n.2782-1992C>A
|
|
XM_006724246.4:c.2536-1992C>A
(ARVCF)
|
XP_006724309.1:n.2536-1992C>A
|
|
XM_011530179.3:c.2749-1992C>A
(ARVCF)
|
XP_011528481.1:n.2749-1992C>A
|
|
XM_011530182.3:c.1348-1992C>A
(ARVCF)
|
XP_011528484.1:n.1348-1992C>A
|
|
XM_024452249.1:c.2536-1992C>A
(ARVCF)
|
XP_024308017.1:n.2536-1992C>A
|
|
NM_000754.4:c.*465G>T
(COMT)
MANE Select
|
NP_000745.1:n.*465G>T
|
|
NM_001135161.2:c.*465G>T
(COMT)
|
NP_001128633.1:n.*465G>T
|
|
NM_001135162.2:c.*465G>T
(COMT)
|
NP_001128634.1:n.*465G>T
|
|
NM_001362828.2:c.*465G>T
(COMT)
|
NP_001349757.1:n.*465G>T
|
|
NM_007310.3:c.*465G>T
(COMT)
|
NP_009294.1:n.*465G>T
|
|