ENST00000290866.10:c.3656T>A
MANE Select
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ENSP00000290866.4:p.Leu1219Gln
|
|
ENST00000290863.10:c.1934T>A
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ENSP00000290863.6:p.Leu645Gln
|
|
ENST00000290866.9:c.3656T>A
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ENSP00000290866.4:p.Leu1219Gln
|
|
ENST00000413513.7:c.1811T>A
|
ENSP00000392247.3:p.Leu604Gln
|
|
ENST00000428043.5:c.3656T>A
|
ENSP00000397593.2:p.Leu1219Gln
|
|
ENST00000577418.5:n.666T>A
|
|
|
ENST00000577647.2:c.1934T>A
|
ENSP00000464149.1:p.Leu645Gln
|
|
ENST00000578839.5:c.*1411T>A
|
ENSP00000462110.2:n.*1411T>A
|
|
ENST00000579314.5:c.*1385T>A
|
ENSP00000462599.1:n.*1385T>A
|
|
ENST00000579409.1:c.343T>A
|
|
|
ENST00000582244.1:n.530T>A
|
|
|
NM_000789.3:c.3656T>A
|
NP_000780.1:p.Leu1219Gln
|
|
NM_001178057.1:c.1811T>A
|
NP_001171528.1:p.Leu604Gln
|
|
NM_152830.2:c.1934T>A
|
NP_690043.1:p.Leu645Gln
|
|
XM_005257110.1:c.3107T>A
|
XP_005257167.1:p.Leu1036Gln
|
|
XM_006721737.2:c.1994T>A
|
XP_006721800.2:p.Leu665Gln
|
|
XM_006721737.3:c.1994T>A
|
XP_006721800.2:p.Leu665Gln
|
|
NM_000789.4:c.3656T>A
MANE Select
|
NP_000780.1:p.Leu1219Gln
|
|
NM_001178057.2:c.1811T>A
|
NP_001171528.1:p.Leu604Gln
|
|
NM_152830.3:c.1934T>A
|
NP_690043.1:p.Leu645Gln
|
|
NM_001382700.1:c.3089T>A
|
NP_001369629.1:p.Leu1030Gln
|
|
NM_001382701.1:c.2804T>A
|
NP_001369630.1:p.Leu935Gln
|
|
NM_001382702.1:c.1271T>A
|
NP_001369631.1:p.Leu424Gln
|
|
NR_168483.1:n.2034T>A
|
|
|