ENST00000304895.9:c.1889C>G
MANE Select
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ENSP00000302728.4:p.Ala630Gly
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ENST00000304895.8:c.1889C>G
|
ENSP00000302728.4:p.Ala630Gly
|
|
ENST00000421103.5:c.1451C>G
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ENSP00000391390.1:p.Ala484Gly
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ENST00000430730.5:c.*1156C>G
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ENSP00000411859.1:n.*1156C>G
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ENST00000447929.5:c.*1269C>G
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ENSP00000411262.1:n.*1269C>G
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ENST00000466883.5:n.2279C>G
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NM_000181.3:c.1889C>G
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NP_000172.2:p.Ala630Gly
|
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NM_001284290.1:c.1451C>G
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NP_001271219.1:p.Ala484Gly
|
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NM_001293104.1:c.1319C>G
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NP_001280033.1:p.Ala440Gly
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NM_001293105.1:c.1232C>G
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NP_001280034.1:p.Ala411Gly
|
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NR_120531.1:n.1935C>G
|
|
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XM_005250297.3:c.1736C>G
|
XP_005250354.1:p.Ala579Gly
|
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XM_011516113.1:c.1388C>G
|
XP_011514415.1:p.Ala463Gly
|
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XM_011516114.1:c.1217C>G
|
XP_011514416.1:p.Ala406Gly
|
|
XM_005250297.4:c.1736C>G
|
XP_005250354.1:p.Ala579Gly
|
|
XM_011516114.2:c.1217C>G
|
XP_011514416.1:p.Ala406Gly
|
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XM_017012091.1:c.1235C>G
|
XP_016867580.1:p.Ala412Gly
|
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XM_017012092.1:c.1166C>G
|
XP_016867581.1:p.Ala389Gly
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XM_017012093.2:c.1064C>G
|
XP_016867582.1:p.Ala355Gly
|
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XR_001744658.2:n.1696C>G
|
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XR_001744659.2:n.1809C>G
|
|
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XR_001744660.2:n.1741C>G
|
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XR_001744661.2:n.1656C>G
|
|
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XR_927461.3:n.1894C>G
|
|
|
NM_000181.4:c.1889C>G
MANE Select
|
NP_000172.2:p.Ala630Gly
|
|
NM_001284290.2:c.1451C>G
|
NP_001271219.1:p.Ala484Gly
|
|
NM_001293104.2:c.1319C>G
|
NP_001280033.1:p.Ala440Gly
|
|
NM_001293105.2:c.1232C>G
|
NP_001280034.1:p.Ala411Gly
|
|
NR_120531.2:n.1834C>G
|
|
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