ENST00000688602.1:c.1427A>C
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|
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ENST00000689936.1:c.1409A>C
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|
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ENST00000359596.8:c.13017A>C
MANE Select
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ENSP00000352608.2:p.Ala4339=
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ENST00000355481.8:c.13002A>C
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ENSP00000347667.3:p.Ala4334=
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ENST00000359596.7:c.13017A>C
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ENSP00000352608.2:p.Ala4339=
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ENST00000360985.7:c.12999A>C
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ENSP00000354254.4:p.Ala4333=
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NM_000540.2:c.13017A>C , LRG_766t1:c.13017A>C
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NP_000531.2:p.Ala4339=
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NM_001042723.1:c.13002A>C
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NP_001036188.1:p.Ala4334=
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XM_006723317.1:c.12999A>C
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XP_006723380.1:p.Ala4333=
|
|
XM_006723319.1:c.12984A>C
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XP_006723382.1:p.Ala4328=
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XM_011527204.1:c.13014A>C
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XP_011525506.1:p.Ala4338=
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XM_011527205.1:c.13017A>C
|
XP_011525507.1:p.Ala4339=
|
|
XM_006723317.2:c.12999A>C
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XP_006723380.1:p.Ala4333=
|
|
XM_006723319.2:c.12984A>C
|
XP_006723382.1:p.Ala4328=
|
|
XM_011527205.2:c.13017A>C
|
XP_011525507.1:p.Ala4339=
|
|
NM_000540.3:c.13017A>C
MANE Select
|
NP_000531.2:p.Ala4339=
|
|
NM_001042723.2:c.13002A>C
|
NP_001036188.1:p.Ala4334=
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