ENST00000298139.7:c.3703A>G
MANE Select
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ENSP00000298139.5:p.Ser1235Gly
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ENST00000650667.1:c.*3317A>G
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ENSP00000498593.1:n.*3317A>G
|
|
ENST00000298139.5:c.3703A>G
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ENSP00000298139.5:p.Ser1235Gly
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ENST00000521620.5:n.2336A>G
|
|
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NM_000553.4:c.3703A>G , LRG_524t1:c.3703A>G
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NP_000544.2:p.Ser1235Gly
|
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XM_011544639.1:c.3622A>G
|
XP_011542941.1:p.Ser1208Gly
|
|
XM_011544640.1:c.2104A>G
|
XP_011542942.1:p.Ser702Gly
|
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XR_949470.1:n.3976A>G
|
|
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XR_949471.1:n.3976A>G
|
|
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XR_949472.1:n.3976A>G
|
|
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XR_949643.1:n.457-5974T>C
|
|
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XR_949644.1:n.381-5974T>C
|
|
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XR_949647.1:n.1070-5974T>C
|
|
|
XR_949648.1:n.972-5974T>C
|
|
|
NM_000553.5:c.3703A>G
|
NP_000544.2:p.Ser1235Gly
|
|
XM_011544639.3:c.3622A>G
|
XP_011542941.1:p.Ser1208Gly
|
|
XM_024447265.1:c.3493A>G
|
XP_024303033.1:p.Ser1165Gly
|
|
XR_949470.3:n.4004A>G
|
|
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XR_949471.3:n.4004A>G
|
|
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XR_949472.3:n.4004A>G
|
|
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NM_000553.6:c.3703A>G
MANE Select
|
NP_000544.2:p.Ser1235Gly
|
|