ENST00000368666.7:c.1034G>A
MANE Select
|
ENSP00000357655.4:p.Gly345Glu
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ENST00000639360.1:c.935G>A
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ENSP00000491774.1:p.Gly312Glu
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|
ENST00000230529.9:c.1034G>A
|
ENSP00000230529.5:p.Gly345Glu
|
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ENST00000361714.5:c.1034G>A
|
ENSP00000354734.2:p.Gly345Glu
|
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ENST00000368663.4:c.*340G>A
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ENSP00000357652.4:n.*340G>A
|
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ENST00000368664.7:c.*438G>A
|
ENSP00000357653.3:n.*438G>A
|
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ENST00000368666.6:c.1088G>A
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ENSP00000357655.3:p.Gly363Glu
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ENST00000409166.5:c.362G>A
|
ENSP00000386467.1:p.Gly121Glu
|
|
ENST00000454589.5:c.*438G>A
|
ENSP00000395928.1:n.*438G>A
|
|
ENST00000604763.5:c.1034G>A
|
ENSP00000473777.1:p.Gly345Glu
|
|
ENST00000613648.1:n.869G>A
|
|
|
ENST00000620524.3:n.965G>A
|
|
|
NM_003880.3:c.1034G>A
|
NP_003871.1:p.Gly345Glu
|
|
NM_198239.1:c.1088G>A
|
NP_937882.1:p.Gly363Glu
|
|
NR_125353.1:n.1288G>A
|
|
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NR_125354.1:n.1208G>A
|
|
|
XM_011536220.1:c.1034G>A
|
XP_011534522.1:p.Gly345Glu
|
|
XM_011536221.1:c.*438G>A
|
XP_011534523.1:n.*438G>A
|
|
XM_011536223.1:c.452G>A
|
XP_011534525.1:p.Gly151Glu
|
|
XM_011536223.3:c.452G>A
|
XP_011534525.1:p.Gly151Glu
|
|
XR_001743705.1:n.1636G>A
|
|
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NM_003880.4:c.1034G>A
|
NP_003871.1:p.Gly345Glu
|
|
NM_198239.2:c.1034G>A
MANE Select
|
NP_937882.2:p.Gly345Glu
|
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NR_125353.2:n.1352G>A
|
|
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NR_125354.3:n.1179G>A
|
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