ENST00000237596.7:c.2239G>T
MANE Select
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ENSP00000237596.2:p.Gly747Trp
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ENST00000237596.6:c.2239G>T
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ENSP00000237596.2:p.Gly747Trp
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ENST00000502363.1:c.493G>T
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ENSP00000425289.1:p.Gly165Trp
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ENST00000508588.5:c.493G>T
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ENSP00000427131.1:p.Gly165Trp
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ENST00000511337.5:n.491G>T
|
|
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ENST00000512858.1:n.451G>T
|
|
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NM_000297.3:c.2239G>T
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NP_000288.1:p.Gly747Trp
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XM_011532028.1:c.2014G>T
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XP_011530330.1:p.Gly672Trp
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XM_011532029.1:c.1519G>T
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XP_011530331.1:p.Gly507Trp
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XM_011532030.1:c.1399G>T
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XP_011530332.1:p.Gly467Trp
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NR_156488.1:n.2205G>T
|
|
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XM_011532028.2:c.2014G>T
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XP_011530330.1:p.Gly672Trp
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XM_011532030.2:c.1399G>T
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XP_011530332.1:p.Gly467Trp
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NM_000297.4:c.2239G>T
MANE Select
|
NP_000288.1:p.Gly747Trp
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NR_156488.2:n.2217G>T
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