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NM_000147.5:c.691G>A
MANE Select
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NP_000138.2:p.Gly231Arg
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ENST00000374479.4:c.691G>A
MANE Select
|
ENSP00000363603.3:p.Gly231Arg
|
|
NM_000147.4:c.691G>A
|
NP_000138.2:p.Gly231Arg
|
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NR_174379.1:n.869G>A
|
|
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NR_174380.1:n.918G>A
|
|
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NR_174381.1:n.757G>A
|
|
|
NR_174382.1:n.1154G>A
|
|
|
ENST00000374479.3:c.691G>A
|
ENSP00000363603.3:p.Gly231Arg
|
|
XM_005245821.1:c.316G>A
|
XP_005245878.1:p.Gly106Arg
|
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XM_005245821.3:c.316G>A
|
XP_005245878.1:p.Gly106Arg
|
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XM_011541167.1:c.58G>A
|
XP_011539469.1:p.Gly20Arg
|
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XM_011541167.3:c.58G>A
|
XP_011539469.1:p.Gly20Arg
|
|
XM_017000905.2:c.388G>A
|
XP_016856394.1:p.Gly130Arg
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