ENST00000252029.8:c.1327_1347delinsGACGGCCCCGCGCTCAGCGGC
(TYMP)
MANE Select
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ENSP00000252029.3:p.Asp443=
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ENST00000395680.6:c.1327_1347delinsGACGGCCCCGCGCTCAGCGGC
(TYMP)
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ENSP00000379037.1:p.Asp443=
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ENST00000395681.6:c.1342_1362delinsGACGGCCCCGCGCTCAGCGGC
(TYMP)
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ENSP00000379038.1:p.Asp448=
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ENST00000543927.6:c.-14+354_-14+374delinsGACGGCCCCGCGCTCAGCGGC
(SCO2)
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ENSP00000444433.1:n.-14+354_-14+374delinsGACGGCCCCGCGCTCAGCGG...
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ENST00000638598.2:c.-14+109_-14+129delinsGACGGCCCCGCGCTCAGCGGC
(SCO2)
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ENSP00000491753.2:n.-14+109_-14+129delinsGACGGCCCCGCGCTCAGCGG...
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ENST00000651490.1:c.119_139delinsGACGGCCCCGCGCTCAGCGGC
(TYMP)
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ENST00000652401.1:c.828_848delinsGACGGCCCCGCGCTCAGCGGC
(TYMP)
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ENST00000252029.7:c.1327_1347delinsGACGGCCCCGCGCTCAGCGGC
(TYMP)
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ENSP00000252029.3:p.Asp443=
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ENST00000395678.7:c.1327_1347delinsGACGGCCCCGCGCTCAGCGGC
(TYMP)
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ENSP00000379036.3:p.Asp443=
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ENST00000395680.5:c.1327_1347delinsGACGGCCCCGCGCTCAGCGGC
(TYMP)
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ENSP00000379037.1:p.Asp443=
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ENST00000395681.5:c.1342_1362delinsGACGGCCCCGCGCTCAGCGGC
(TYMP)
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ENSP00000379038.1:p.Asp448=
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ENST00000423348.1:c.-14+354_-14+374delinsGACGGCCCCGCGCTCAGCGGC
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ENSP00000403570.1:n.-14+354_-14+374delinsGACGGCCCCGCGCTCAGCGG...
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ENST00000425169.1:c.1228_1248delinsGACGGCCCCGCGCTCAGCGGC
(TYMP)
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ENSP00000395875.1:p.Asp410=
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ENST00000439934.5:c.-14+109_-14+129delinsGACGGCCCCGCGCTCAGCGGC
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ENSP00000415642.1:n.-14+109_-14+129delinsGACGGCCCCGCGCTCAGCGG...
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ENST00000476284.1:n.1437_1457delinsGACGGCCCCGCGCTCAGCGGC
(TYMP)
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ENST00000487577.5:n.1614_1634delinsGACGGCCCCGCGCTCAGCGGC
(TYMP)
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ENST00000535425.5:c.-14+109_-14+129delinsGACGGCCCCGCGCTCAGCGGC
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ENSP00000444242.1:n.-14+109_-14+129delinsGACGGCCCCGCGCTCAGCGG...
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ENST00000543927.5:c.-14+354_-14+374delinsGACGGCCCCGCGCTCAGCGGC
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ENSP00000444433.1:n.-14+354_-14+374delinsGACGGCCCCGCGCTCAGCGG...
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NM_001113755.2:c.1327_1347delinsGACGGCCCCGCGCTCAGCGGC
(TYMP)
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NP_001107227.1:p.Asp443=
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NM_001113756.2:c.1327_1347delinsGACGGCCCCGCGCTCAGCGGC
(TYMP)
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NP_001107228.1:p.Asp443=
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NM_001169109.1:c.-14+354_-14+374delinsGACGGCCCCGCGCTCAGCGGC
(SCO2)
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NP_001162580.1:n.-14+354_-14+374delinsGACGGCCCCGCGCTCAGCGGC
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NM_001169110.1:c.-14+109_-14+129delinsGACGGCCCCGCGCTCAGCGGC
(SCO2)
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NP_001162581.1:n.-14+109_-14+129delinsGACGGCCCCGCGCTCAGCGGC
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NM_001257988.1:c.1327_1347delinsGACGGCCCCGCGCTCAGCGGC , LRG_727t1:c.1327_1347delinsGACGGCCCCGCGCTCAGCGGC
(TYMP)
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NP_001244917.1:p.Asp443=
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NM_001257989.1:c.1342_1362delinsGACGGCCCCGCGCTCAGCGGC , LRG_727t2:c.1342_1362delinsGACGGCCCCGCGCTCAGCGGC
(TYMP)
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NP_001244918.1:p.Asp448=
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NM_001953.4:c.1327_1347delinsGACGGCCCCGCGCTCAGCGGC
(TYMP)
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NP_001944.1:p.Asp443=
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NM_001113755.3:c.1327_1347delinsGACGGCCCCGCGCTCAGCGGC
(TYMP)
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NP_001107227.1:p.Asp443=
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NM_001113756.3:c.1327_1347delinsGACGGCCCCGCGCTCAGCGGC
(TYMP)
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NP_001107228.1:p.Asp443=
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NM_001953.5:c.1327_1347delinsGACGGCCCCGCGCTCAGCGGC
(TYMP)
MANE Select
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NP_001944.1:p.Asp443=
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NM_001169109.2:c.-14+354_-14+374delinsGACGGCCCCGCGCTCAGCGGC
(SCO2)
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NP_001162580.1:n.-14+354_-14+374delinsGACGGCCCCGCGCTCAGCGGC
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