ENST00000375076.9:c.1101A>T
MANE Select
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ENSP00000364217.4:p.Gln367His
|
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ENST00000375055.6:c.*30-129A>T
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ENSP00000364195.2:n.*30-129A>T
|
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ENST00000375065.6:c.288A>T
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ENSP00000364206.6:p.Gln96His
|
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ENST00000375067.7:c.946A>T
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ENSP00000364208.3:p.Thr316Ser
|
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ENST00000375069.7:c.1149A>T
|
ENSP00000364210.4:p.Gln383His
|
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ENST00000375070.7:c.771A>T
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ENSP00000364211.4:p.Gln257His
|
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ENST00000375076.8:c.1101A>T
|
ENSP00000364217.4:p.Gln367His
|
|
ENST00000438221.6:c.*30-129A>T
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ENSP00000387887.2:n.*30-129A>T
|
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ENST00000469940.5:n.268A>T
|
|
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ENST00000473619.5:n.643A>T
|
|
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ENST00000484849.5:n.1308A>T
|
|
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ENST00000488669.5:n.616-129A>T
|
|
|
ENST00000620802.4:c.348A>T
|
ENSP00000484081.1:p.Gln116His
|
|
NM_001136.4:c.1101A>T
|
NP_001127.1:p.Gln367His
|
|
NM_001206929.1:c.1149A>T
|
NP_001193858.1:p.Gln383His
|
|
NM_001206932.1:c.1059A>T
|
NP_001193861.1:p.Gln353His
|
|
NM_001206934.1:c.*30-129A>T
|
NP_001193863.1:n.*30-129A>T
|
|
NM_001206936.1:c.1022-129A>T
|
NP_001193865.1:n.1022-129A>T
|
|
NM_001206940.1:c.*30-129A>T
|
NP_001193869.1:n.*30-129A>T
|
|
NM_001206954.1:c.932-129A>T
|
NP_001193883.1:n.932-129A>T
|
|
NM_001206966.1:c.*29+156A>T
|
NP_001193895.1:n.*29+156A>T
|
|
NM_172197.2:c.946A>T
|
NP_751947.1:p.Thr316Ser
|
|
NR_038190.1:n.1384A>T
|
|
|
XM_017010328.2:c.1073-129A>T
|
XP_016865817.1:n.1073-129A>T
|
|
XR_001743189.2:n.1165A>T
|
|
|
XR_001743190.2:n.1117A>T
|
|
|
NM_001136.5:c.1101A>T
MANE Select
|
NP_001127.1:p.Gln367His
|
|
NM_001206932.2:c.1059A>T
|
NP_001193861.1:p.Gln353His
|
|
NM_001206936.2:c.1022-129A>T
|
NP_001193865.1:n.1022-129A>T
|
|
NM_001206940.2:c.*30-129A>T
|
NP_001193869.1:n.*30-129A>T
|
|
NM_001206954.2:c.932-129A>T
|
NP_001193883.1:n.932-129A>T
|
|
NM_001206966.2:c.*29+156A>T
|
NP_001193895.1:n.*29+156A>T
|
|
NM_172197.3:c.946A>T
|
NP_751947.1:p.Thr316Ser
|
|
NR_038190.2:n.1315A>T
|
|
|
NM_001206929.2:c.1149A>T
|
NP_001193858.1:p.Gln383His
|
|
NM_001206934.2:c.*30-129A>T
|
NP_001193863.1:n.*30-129A>T
|
|