ENST00000265517.10:c.2676A>C
MANE Select
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ENSP00000265517.5:p.Gly892=
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ENST00000457717.6:c.2676A>C
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ENSP00000400821.1:p.Gly892=
|
|
ENST00000511045.6:c.2427A>C
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ENSP00000427679.2:p.Gly809=
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ENST00000265517.9:c.2676A>C
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ENSP00000265517.5:p.Gly892=
|
|
ENST00000457717.5:c.2676A>C
|
ENSP00000400821.1:p.Gly892=
|
|
ENST00000511045.5:c.2757A>C
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ENSP00000427679.1:p.Gly919=
|
|
ENST00000619629.1:c.*1123A>C
|
ENSP00000482850.1:n.*1123A>C
|
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NM_000253.3:c.2676A>C
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NP_000244.2:p.Gly892=
|
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NM_001300785.1:c.2757A>C
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NP_001287714.1:p.Gly919=
|
|
NM_000253.4:c.2676A>C
|
NP_000244.2:p.Gly892=
|
|
NM_001300785.2:c.2427A>C
|
NP_001287714.2:p.Gly809=
|
|
NM_001386140.1:c.2676A>C
MANE Select
|
NP_001373069.1:p.Gly892=
|
|