ENST00000330684.4:c.2765C>G
MANE Select
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ENSP00000332549.3:p.Ala922Gly
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ENST00000535259.6:c.2294C>G
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ENSP00000441572.3:p.Ala765Gly
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ENST00000636273.2:n.2358C>G
|
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ENST00000674742.1:c.2294C>G
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ENSP00000502200.1:p.Ala765Gly
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ENST00000675398.1:c.*135C>G
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ENSP00000502752.1:n.*135C>G
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ENST00000330684.3:c.2765C>G
|
ENSP00000332549.3:p.Ala922Gly
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ENST00000396573.6:c.2765C>G
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ENSP00000379818.2:p.Ala922Gly
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ENST00000396575.6:c.2354C>G
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ENSP00000379820.3:p.Ala785Gly
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ENST00000461292.3:n.2404C>G
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ENST00000535259.5:c.2354C>G
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ENSP00000441572.2:p.Ala785Gly
|
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ENST00000562109.5:c.2765C>G
|
ENSP00000454998.1:p.Ala922Gly
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NM_000833.4:c.2765C>G
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NP_000824.1:p.Ala922Gly
|
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NM_001134407.2:c.2765C>G
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NP_001127879.1:p.Ala922Gly
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NM_001134408.2:c.2765C>G
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NP_001127880.1:p.Ala922Gly
|
|
XM_011522456.1:c.2606C>G
|
XP_011520758.1:p.Ala869Gly
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XM_011522457.1:c.2507C>G
|
XP_011520759.1:p.Ala836Gly
|
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XM_011522458.1:c.2294C>G
|
XP_011520760.1:p.Ala765Gly
|
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XM_011522459.1:c.2294C>G
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XP_011520761.1:p.Ala765Gly
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XM_011522460.1:c.2294C>G
|
XP_011520762.1:p.Ala765Gly
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XM_011522461.1:c.2765C>G
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XP_011520763.1:p.Ala922Gly
|
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XM_011522458.3:c.2294C>G
|
XP_011520760.1:p.Ala765Gly
|
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XM_011522461.3:c.2765C>G
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XP_011520763.1:p.Ala922Gly
|
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XM_017023172.1:c.2921C>G
|
XP_016878661.1:p.Ala974Gly
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XM_017023173.1:c.2921C>G
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XP_016878662.1:p.Ala974Gly
|
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NM_001134407.3:c.2765C>G
MANE Select
|
NP_001127879.1:p.Ala922Gly
|
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NM_000833.5:c.2765C>G
|
NP_000824.1:p.Ala922Gly
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