ENST00000298139.7:c.3139G>A
MANE Select
|
ENSP00000298139.5:p.Gly1047Ser
|
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ENST00000650667.1:c.*2753G>A
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ENSP00000498593.1:n.*2753G>A
|
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ENST00000298139.5:c.3139G>A
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ENSP00000298139.5:p.Gly1047Ser
|
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ENST00000521620.5:n.1772G>A
|
|
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NM_000553.4:c.3139G>A , LRG_524t1:c.3139G>A
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NP_000544.2:p.Gly1047Ser
|
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XM_011544639.1:c.3058G>A
|
XP_011542941.1:p.Gly1020Ser
|
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XM_011544640.1:c.1540G>A
|
XP_011542942.1:p.Gly514Ser
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XR_949470.1:n.3412G>A
|
|
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XR_949471.1:n.3412G>A
|
|
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XR_949472.1:n.3412G>A
|
|
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NM_000553.5:c.3139G>A
|
NP_000544.2:p.Gly1047Ser
|
|
XM_011544639.3:c.3058G>A
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XP_011542941.1:p.Gly1020Ser
|
|
XM_024447265.1:c.2929G>A
|
XP_024303033.1:p.Gly977Ser
|
|
XR_949470.3:n.3440G>A
|
|
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XR_949471.3:n.3440G>A
|
|
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XR_949472.3:n.3440G>A
|
|
|
NM_000553.6:c.3139G>A
MANE Select
|
NP_000544.2:p.Gly1047Ser
|
|