ENST00000371270.6:c.1331A>G
MANE Select
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ENSP00000360317.3:p.Glu444Gly
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ENST00000371270.5:c.1331A>G
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ENSP00000360317.3:p.Glu444Gly
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ENST00000490994.6:c.*1117A>G
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ENSP00000433314.1:n.*1117A>G
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ENST00000525991.5:c.*906A>G
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ENSP00000433842.1:n.*906A>G
|
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ENST00000526814.5:n.1586A>G
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ENST00000527420.5:c.*188A>G
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ENSP00000433191.1:n.*188A>G
|
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ENST00000527953.5:n.1625A>G
|
|
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ENST00000531714.1:n.519A>G
|
|
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ENST00000533320.5:n.1565A>G
|
|
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ENST00000535898.5:c.1025A>G
|
ENSP00000445062.1:p.Glu342Gly
|
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ENST00000539050.5:c.1121A>G
|
ENSP00000442343.2:p.Glu374Gly
|
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ENST00000623108.3:c.1121A>G
|
ENSP00000485110.1:p.Glu374Gly
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|
NM_000770.3:c.1331A>G
MANE Select
|
NP_000761.3:p.Glu444Gly
|
|
NM_001198853.1:c.1121A>G
|
NP_001185782.1:p.Glu374Gly
|
|
NM_001198854.1:c.1025A>G
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NP_001185783.1:p.Glu342Gly
|
|
NM_001198855.1:c.1121A>G
|
NP_001185784.1:p.Glu374Gly
|
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XR_945610.1:n.1466A>G
|
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