ENST00000378043.9:c.923A>G
MANE Select
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ENSP00000367282.4:p.Asn308Ser
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ENST00000378043.8:c.923A>G
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ENSP00000367282.4:p.Asn308Ser
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ENST00000449131.6:c.743A>G
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ENSP00000399709.2:p.Asn248Ser
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ENST00000524877.5:n.2554A>G
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|
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ENST00000524926.5:c.1126A>G
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ENSP00000432681.1:p.Thr376Ala
|
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ENST00000526988.1:c.808A>G
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ENSP00000433195.1:p.Thr270Ala
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ENST00000534553.5:c.164-2702A>G
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ENSP00000431189.1:n.164-2702A>G
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NM_001139443.1:c.743A>G
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NP_001132915.1:p.Asn248Ser
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NM_001300786.1:c.688-339A>G
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NP_001287715.1:n.688-339A>G
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NM_001300787.1:c.743A>G
|
NP_001287716.1:p.Asn248Ser
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NM_004183.3:c.923A>G
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NP_004174.1:p.Asn308Ser
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XM_005274210.2:c.923A>G
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XP_005274267.1:p.Asn308Ser
|
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XM_005274215.2:c.605A>G
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XP_005274272.1:p.Asn202Ser
|
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XM_005274216.2:c.946A>G
|
XP_005274273.1:p.Thr316Ala
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XM_005274218.3:c.808A>G
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XP_005274275.1:p.Thr270Ala
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|
XM_005274219.2:c.867+1255A>G
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XP_005274276.1:n.867+1255A>G
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XM_005274221.2:c.714+2089A>G
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XP_005274278.1:n.714+2089A>G
|
|
XM_011545229.1:c.923A>G
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XP_011543531.1:p.Asn308Ser
|
|
XM_011545230.1:c.830A>G
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XP_011543532.1:p.Asn277Ser
|
|
XM_011545231.1:c.605A>G
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XP_011543533.1:p.Asn202Ser
|
|
XM_011545232.1:c.1126A>G
|
XP_011543534.1:p.Thr376Ala
|
|
XM_011545233.1:c.80A>G
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XP_011543535.1:p.Asn27Ser
|
|
NM_001363591.1:c.605A>G
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NP_001350520.1:p.Asn202Ser
|
|
NM_001363592.1:c.1126A>G
|
NP_001350521.1:p.Thr376Ala
|
|
NM_001363593.1:c.-50A>G
|
NP_001350522.1:n.-50A>G
|
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NR_134580.1:n.1706A>G
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|
|
XM_005274210.4:c.923A>G
|
XP_005274267.1:p.Asn308Ser
|
|
XM_005274215.4:c.605A>G
|
XP_005274272.1:p.Asn202Ser
|
|
XM_005274216.4:c.946A>G
|
XP_005274273.1:p.Thr316Ala
|
|
XM_005274219.4:c.867+1255A>G
|
XP_005274276.1:n.867+1255A>G
|
|
XM_005274221.4:c.714+2089A>G
|
XP_005274278.1:n.714+2089A>G
|
|
XM_011545229.3:c.923A>G
|
XP_011543531.1:p.Asn308Ser
|
|
XM_011545230.3:c.830A>G
|
XP_011543532.1:p.Asn277Ser
|
|
XM_011545233.3:c.80A>G
|
XP_011543535.1:p.Asn27Ser
|
|
XM_017018230.2:c.808A>G
|
XP_016873719.1:p.Thr270Ala
|
|
XR_001747952.2:n.1624A>G
|
|
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XR_001747953.2:n.1557+1255A>G
|
|
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XR_001747954.2:n.1404+2089A>G
|
|
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XR_001748245.1:n.196+179T>C
|
|
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XR_002957249.1:n.196+179T>C
|
|
|
NM_004183.4:c.923A>G
MANE Select
|
NP_004174.1:p.Asn308Ser
|
|
NM_001139443.2:c.743A>G
|
NP_001132915.1:p.Asn248Ser
|
|
NM_001300786.2:c.688-339A>G
|
NP_001287715.1:n.688-339A>G
|
|
NM_001300787.2:c.743A>G
|
NP_001287716.1:p.Asn248Ser
|
|
NM_001363591.2:c.605A>G
|
NP_001350520.1:p.Asn202Ser
|
|
NM_001363593.2:c.-50A>G
|
NP_001350522.1:n.-50A>G
|
|
NR_134580.2:n.1239A>G
|
|
|