|
ENST00000016171.6:c.*1153G>T
(COX15)
MANE Select
|
ENSP00000016171.6:n.*1153G>T
|
|
|
ENST00000649102.1:c.*460+2914G>T
|
ENSP00000497114.1:n.*460+2914G>T
|
|
|
ENST00000370483.9:c.1147G>T
(COX15)
|
ENSP00000359514.5:p.Glu383Ter
|
|
|
ENST00000493385.5:n.117-9484C>A
(CUTC)
|
|
|
|
NM_004376.5:c.1147G>T , LRG_406t2:c.1147G>T
(COX15)
|
NP_004367.2:p.Glu383Ter
|
|
|
NM_078470.4:c.*1153G>T , LRG_406t1:c.*1153G>T
(COX15)
|
NP_510870.1:n.*1153G>T
|
|
|
XM_005269539.3:c.1101+2914G>T
(COX15)
|
XP_005269596.1:n.1101+2914G>T
|
|
|
XM_006717633.2:c.*1334G>T
(COX15)
|
XP_006717696.1:n.*1334G>T
|
|
|
XM_006717634.2:c.*49+2914G>T
(COX15)
|
XP_006717697.1:n.*49+2914G>T
|
|
|
XM_011539298.1:c.*95G>T
(COX15)
|
XP_011537600.1:n.*95G>T
|
|
|
NM_001320974.1:c.1101+2914G>T
(COX15)
|
NP_001307903.1:n.1101+2914G>T
|
|
|
NM_001320975.1:c.*1334G>T
(COX15)
|
NP_001307904.1:n.*1334G>T
|
|
|
NM_001320976.1:c.*1153G>T
(COX15)
|
NP_001307905.1:n.*1153G>T
|
|
|
NM_004376.6:c.1147G>T
(COX15)
|
NP_004367.2:p.Glu383Ter
|
|
|
NM_078470.5:c.*1153G>T
(COX15)
|
NP_510870.1:n.*1153G>T
|
|
|
XM_006717634.3:c.*49+2914G>T
(COX15)
|
XP_006717697.1:n.*49+2914G>T
|
|
|
XM_011539298.2:c.*95G>T
(COX15)
|
XP_011537600.1:n.*95G>T
|
|
|
NM_001320974.2:c.1101+2914G>T
(COX15)
|
NP_001307903.1:n.1101+2914G>T
|
|
|
NM_001320975.2:c.*1334G>T
(COX15)
|
NP_001307904.1:n.*1334G>T
|
|
|
NM_001320976.2:c.*1153G>T
(COX15)
|
NP_001307905.1:n.*1153G>T
|
|
|
NM_001372024.1:c.*372G>T
(COX15)
|
NP_001358953.1:n.*372G>T
|
|
|
NM_001372025.1:c.*1153G>T
(COX15)
|
NP_001358954.1:n.*1153G>T
|
|
|
NM_001372026.1:c.*1153G>T
(COX15)
|
NP_001358955.1:n.*1153G>T
|
|
|
NM_001372027.1:c.*1257G>T
(COX15)
|
NP_001358956.1:n.*1257G>T
|
|
|
NM_001372028.1:c.*580G>T
(COX15)
|
NP_001358957.1:n.*580G>T
|
|
|
NM_004376.7:c.1147G>T
(COX15)
|
NP_004367.2:p.Glu383Ter
|
|
|
NM_078470.6:c.*1153G>T
(COX15)
MANE Select
|
NP_510870.1:n.*1153G>T
|
|
|
NR_164009.1:n.2226G>T
(COX15)
|
|
|
