ENST00000288840.10:c.1046T>G
MANE Select
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ENSP00000288840.5:p.Val349Gly
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ENST00000288840.9:c.1046T>G
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ENSP00000288840.5:p.Val349Gly
|
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ENST00000557916.5:c.1178T>G
|
ENSP00000452955.1:n.1178T>G
|
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ENST00000559931.5:c.350T>G
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ENSP00000453446.1:n.350T>G
|
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NM_005585.4:c.1046T>G
|
NP_005576.3:p.Val349Gly
|
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NR_027654.1:n.2101T>G
|
|
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XM_011521561.1:c.263T>G
|
XP_011519863.1:p.Val88Gly
|
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XR_931825.1:n.2445T>G
|
|
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XM_011521561.2:c.263T>G
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XP_011519863.1:p.Val88Gly
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NM_005585.5:c.1046T>G
MANE Select
|
NP_005576.3:p.Val349Gly
|
|
NR_027654.2:n.2201T>G
|
|
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