ENST00000225964.10:c.3187A>C
MANE Select
|
ENSP00000225964.6:p.Ser1063Arg
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ENST00000225964.9:c.3187A>C
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ENSP00000225964.5:p.Ser1063Arg
|
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ENST00000486572.1:n.5A>C
|
|
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ENST00000511732.1:n.131A>C
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|
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NM_000088.3:c.3187A>C , LRG_1t1:c.3187A>C
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NP_000079.2:p.Ser1063Arg
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|
XM_005257058.3:c.2917A>C
|
XP_005257115.2:p.Ser973Arg
|
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XM_005257059.3:c.2269A>C
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XP_005257116.2:p.Ser757Arg
|
|
XM_011524341.1:c.2989A>C
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XP_011522643.1:p.Ser997Arg
|
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XM_005257058.4:c.2917A>C
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XP_005257115.2:p.Ser973Arg
|
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XM_005257059.4:c.2269A>C
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XP_005257116.2:p.Ser757Arg
|
|
NM_000088.4:c.3187A>C
MANE Select
|
NP_000079.2:p.Ser1063Arg
|
|