ENST00000623535.2:c.2861A>C
MANE Select
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ENSP00000485244.1:p.Asp954Ala
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ENST00000674046.1:c.2984A>C
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ENSP00000501174.1:p.Asp995Ala
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ENST00000379989.6:c.2713+148A>C
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ENSP00000369325.3:n.2713+148A>C
|
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ENST00000379996.7:c.2713+148A>C
|
ENSP00000369332.3:n.2713+148A>C
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ENST00000623535.1:c.2861A>C
|
ENSP00000485244.1:p.Asp954Ala
|
|
NM_001037343.1:c.2713+148A>C
|
NP_001032420.1:n.2713+148A>C
|
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NM_003159.2:c.2713+148A>C
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NP_003150.1:n.2713+148A>C
|
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XM_011545569.1:c.2785+148A>C
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XP_011543871.1:n.2785+148A>C
|
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XM_011545570.1:c.2704+148A>C
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XP_011543872.1:n.2704+148A>C
|
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XR_950484.1:n.3088+148A>C
|
|
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NM_001323289.1:c.2861A>C
|
NP_001310218.1:p.Asp954Ala
|
|
NM_001323289.2:c.2861A>C
MANE Select
|
NP_001310218.1:p.Asp954Ala
|
|
NM_001037343.2:c.2713+148A>C
|
NP_001032420.1:n.2713+148A>C
|
|
NM_003159.3:c.2713+148A>C
|
NP_003150.1:n.2713+148A>C
|
|