ENST00000264595.7:c.559A>G
MANE Select
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ENSP00000264595.2:p.Ile187Val
|
|
ENST00000264595.6:c.559A>G
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ENSP00000264595.2:p.Ile187Val
|
|
ENST00000502310.5:c.214A>G
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ENSP00000423798.1:p.Ile72Val
|
|
ENST00000506853.5:n.593A>G
|
|
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ENST00000510635.1:c.255A>G
|
|
|
ENST00000510955.5:n.480A>G
|
|
|
NM_000027.3:c.559A>G
|
NP_000018.2:p.Ile187Val
|
|
NM_001171988.1:c.559A>G
|
NP_001165459.1:p.Ile187Val
|
|
NR_033655.1:n.687A>G
|
|
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XM_006714123.2:c.559A>G
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XP_006714186.1:p.Ile187Val
|
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XR_001741155.2:n.653A>G
|
|
|
NM_000027.4:c.559A>G
MANE Select
|
NP_000018.2:p.Ile187Val
|
|
NM_001171988.2:c.559A>G
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NP_001165459.1:p.Ile187Val
|
|
NR_033655.2:n.621A>G
|
|
|