ENST00000288840.10:c.1001T>G
MANE Select
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ENSP00000288840.5:p.Val334Gly
|
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ENST00000288840.9:c.1001T>G
|
ENSP00000288840.5:p.Val334Gly
|
|
ENST00000557916.5:c.1133T>G
|
ENSP00000452955.1:n.1133T>G
|
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ENST00000559931.5:c.305T>G
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ENSP00000453446.1:n.305T>G
|
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NM_005585.4:c.1001T>G
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NP_005576.3:p.Val334Gly
|
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NR_027654.1:n.2056T>G
|
|
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XM_011521561.1:c.218T>G
|
XP_011519863.1:p.Val73Gly
|
|
XR_931825.1:n.2400T>G
|
|
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XM_011521561.2:c.218T>G
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XP_011519863.1:p.Val73Gly
|
|
NM_005585.5:c.1001T>G
MANE Select
|
NP_005576.3:p.Val334Gly
|
|
NR_027654.2:n.2156T>G
|
|
|