ENST00000515683.6:c.1104-147_1104-142delinsTTGACC
(ADH1C)
MANE Select
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ENSP00000426083.1:n.1104-147_1104-142delinsTTGACC
|
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ENST00000639454.1:c.18+15735_18+15740delinsTTGACC
(ADH1B)
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ENSP00000491622.1:n.18+15735_18+15740delinsTTGACC
|
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ENST00000515683.5:c.1104-147_1104-142delinsTTGACC
(ADH1C)
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ENSP00000426083.1:n.1104-147_1104-142delinsTTGACC
|
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NM_000669.4:c.1104-147_1104-142delinsTTGACC
(ADH1C)
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NP_000660.1:n.1104-147_1104-142delinsTTGACC
|
|
NR_133005.1:n.1430-147_1430-142delinsTTGACC
(ADH1C)
|
|
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XM_011531588.1:c.1002-147_1002-142delinsTTGACC
(ADH1C)
|
XP_011529890.1:n.1002-147_1002-142delinsTTGACC
|
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XM_011531589.1:c.984-147_984-142delinsTTGACC
(ADH1C)
|
XP_011529891.1:n.984-147_984-142delinsTTGACC
|
|
NM_000669.5:c.1104-147_1104-142delinsTTGACC
(ADH1C)
MANE Select
|
NP_000660.1:n.1104-147_1104-142delinsTTGACC
|
|
NR_133005.2:n.1131-147_1131-142delinsTTGACC
(ADH1C)
|
|
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