ENST00000223051.8:c.788G>A
MANE Select
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ENSP00000223051.3:p.Gly263Asp
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ENST00000223051.7:c.788G>A
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ENSP00000223051.3:p.Gly263Asp
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ENST00000431692.5:c.788G>A
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ENSP00000413905.1:p.Gly263Asp
|
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ENST00000462090.5:n.29G>A
|
|
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ENST00000462107.1:c.788G>A
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ENSP00000420525.1:p.Gly263Asp
|
|
ENST00000465294.5:n.793G>A
|
|
|
ENST00000473374.5:n.238G>A
|
|
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ENST00000473571.1:n.242G>A
|
|
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ENST00000475011.1:n.317G>A
|
|
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ENST00000476304.5:n.409G>A
|
|
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ENST00000490084.5:c.43G>A
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|
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NM_001206855.1:c.275G>A
|
NP_001193784.1:p.Gly92Asp
|
|
NM_003227.3:c.788G>A
|
NP_003218.2:p.Gly263Asp
|
|
XM_005250553.3:c.788G>A
|
XP_005250610.1:p.Gly263Asp
|
|
XM_005250554.3:c.788G>A
|
XP_005250611.1:p.Gly263Asp
|
|
NM_001206855.2:c.275G>A
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NP_001193784.1:p.Gly92Asp
|
|
XM_005250553.4:c.788G>A
|
XP_005250610.1:p.Gly263Asp
|
|
XM_017012573.1:c.788G>A
|
XP_016868062.1:p.Gly263Asp
|
|
NM_003227.4:c.788G>A
MANE Select
|
NP_003218.2:p.Gly263Asp
|
|
NM_001206855.3:c.275G>A
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NP_001193784.1:p.Gly92Asp
|
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