ENST00000328195.8:c.231A=
MANE Select
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ENSP00000333551.3:p.Ala77=
|
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ENST00000328195.7:c.231A=
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ENSP00000333551.3:p.Ala77=
|
|
ENST00000518036.5:c.*83A=
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ENSP00000428005.1:n.*83A=
|
|
ENST00000520073.5:n.296A=
|
|
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ENST00000523187.5:c.75A=
|
ENSP00000427886.1:p.Ala25=
|
|
ENST00000523358.5:c.231A=
|
ENSP00000427778.1:p.Ala77=
|
|
ENST00000523994.1:n.236A=
|
|
|
NM_007198.3:c.231A=
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NP_009129.1:p.Ala77=
|
|
NM_001349346.1:c.231A=
|
NP_001336275.1:p.Ala77=
|
|
NM_001349347.1:c.225A=
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NP_001336276.1:p.Ala75=
|
|
NM_001349348.1:c.75A=
|
NP_001336277.1:p.Ala25=
|
|
NM_001349349.1:c.336A=
|
NP_001336278.1:p.Ala112=
|
|
NM_007198.4:c.231A=
MANE Select
|
NP_009129.1:p.Ala77=
|
|
NM_001349346.2:c.231A=
|
NP_001336275.1:p.Ala77=
|
|
NM_001349347.2:c.225A=
|
NP_001336276.1:p.Ala75=
|
|
NM_001349348.2:c.75A=
|
NP_001336277.1:p.Ala25=
|
|