ENST00000317357.10:c.1724G>T
MANE Select
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ENSP00000318900.5:p.Gly575Val
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ENST00000317357.9:c.1724G>T
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ENSP00000318900.5:p.Gly575Val
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NM_018013.3:c.1724G>T
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NP_060483.3:p.Gly575Val
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XM_005267041.3:c.1877G>T
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XP_005267098.1:p.Gly626Val
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XM_005267042.3:c.1781G>T
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XP_005267099.1:p.Gly594Val
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XM_011535920.1:c.1877G>T
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XP_011534222.1:p.Gly626Val
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XM_011535921.1:c.1763G>T
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XP_011534223.1:p.Gly588Val
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XM_011535922.1:c.1136G>T
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XP_011534224.1:p.Gly379Val
|
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XM_011535923.1:c.947G>T
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XP_011534225.1:p.Gly316Val
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XM_005267041.4:c.1877G>T
|
XP_005267098.1:p.Gly626Val
|
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XM_005267042.4:c.1781G>T
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XP_005267099.1:p.Gly594Val
|
|
XM_011535920.2:c.1877G>T
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XP_011534222.1:p.Gly626Val
|
|
XM_011535921.2:c.1763G>T
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XP_011534223.1:p.Gly588Val
|
|
XM_011535923.2:c.947G>T
|
XP_011534225.1:p.Gly316Val
|
|
XM_017010991.1:c.1277G>T
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XP_016866480.1:p.Gly426Val
|
|
XM_017010992.1:c.1277G>T
|
XP_016866481.1:p.Gly426Val
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|
XM_017010993.1:c.1277G>T
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XP_016866482.1:p.Gly426Val
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XM_017010994.1:c.1277G>T
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XP_016866483.1:p.Gly426Val
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NM_018013.4:c.1724G>T
MANE Select
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NP_060483.3:p.Gly575Val
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