ENST00000295897.9:c.1160C>G
MANE Select
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ENSP00000295897.4:p.Ala387Gly
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ENST00000295897.8:c.1160C>G
|
ENSP00000295897.4:p.Ala387Gly
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ENST00000401494.7:c.815C>G
|
ENSP00000384695.3:p.Ala272Gly
|
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ENST00000415165.6:c.584C>G
|
ENSP00000401820.2:p.Ala195Gly
|
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ENST00000476441.6:c.*439C>G
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ENSP00000423727.1:n.*439C>G
|
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ENST00000484992.1:n.480C>G
|
|
|
ENST00000503124.5:c.710C>G
|
ENSP00000421027.1:p.Ala237Gly
|
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ENST00000504043.1:n.163C>G
|
|
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ENST00000505649.5:n.846C>G
|
|
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ENST00000509063.5:c.1160C>G
|
ENSP00000422784.1:p.Ala387Gly
|
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ENST00000511370.1:c.693C>G
|
|
|
ENST00000621085.4:c.521C>G
|
ENSP00000483421.1:p.Ala174Gly
|
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ENST00000621628.4:c.521C>G
|
ENSP00000480485.1:p.Ala174Gly
|
|
NM_000477.5:c.1160C>G
|
NP_000468.1:p.Ala387Gly
|
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NM_000477.6:c.1160C>G
|
NP_000468.1:p.Ala387Gly
|
|
NM_000477.7:c.1160C>G
MANE Select
|
NP_000468.1:p.Ala387Gly
|
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