ENST00000593677.2:c.1177C>T
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|
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ENST00000688602.1:c.2574C>T
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|
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ENST00000689936.1:c.2546C>T
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|
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ENST00000359596.8:c.14241C>T
MANE Select
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ENSP00000352608.2:p.Ala4747=
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ENST00000355481.8:c.14226C>T
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ENSP00000347667.3:p.Ala4742=
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ENST00000359596.7:c.14241C>T
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ENSP00000352608.2:p.Ala4747=
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ENST00000360985.7:c.14223C>T
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ENSP00000354254.4:p.Ala4741=
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NM_000540.2:c.14241C>T , LRG_766t1:c.14241C>T
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NP_000531.2:p.Ala4747=
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NM_001042723.1:c.14226C>T
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NP_001036188.1:p.Ala4742=
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XM_006723317.1:c.14223C>T
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XP_006723380.1:p.Ala4741=
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XM_006723319.1:c.14208C>T
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XP_006723382.1:p.Ala4736=
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XM_011527204.1:c.14238C>T
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XP_011525506.1:p.Ala4746=
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XM_011527205.1:c.14154C>T
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XP_011525507.1:p.Ala4718=
|
|
XM_006723317.2:c.14223C>T
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XP_006723380.1:p.Ala4741=
|
|
XM_006723319.2:c.14208C>T
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XP_006723382.1:p.Ala4736=
|
|
XM_011527205.2:c.14154C>T
|
XP_011525507.1:p.Ala4718=
|
|
NM_000540.3:c.14241C>T
MANE Select
|
NP_000531.2:p.Ala4747=
|
|
NM_001042723.2:c.14226C>T
|
NP_001036188.1:p.Ala4742=
|
|