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ENSP00000500964.2:n.1870-723G=
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ENST00000242839.10:c.2336G=
MANE Select
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ENSP00000242839.5:p.Trp779=
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ENST00000344297.9:c.1870-723G=
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ENSP00000342559.5:n.1870-723G=
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NM_001243182.1:c.2003G=
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XM_005266423.2:c.2240G=
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XP_005266480.1:p.Trp747=
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XP_005266484.1:n.2122-723G=
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XM_005266431.2:c.2300G=
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XP_005266489.1:n.1870-723G=
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XM_006719837.2:c.2240G=
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XP_006719900.1:p.Trp747=
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|
|
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XM_006719839.1:c.152G=
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XP_006719902.1:p.Trp51=
|
|
|
XM_011535117.1:c.2240G=
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XP_011533419.1:p.Trp747=
|
|
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XM_011535118.1:c.2336G=
|
XP_011533420.1:p.Trp779=
|
|
|
XM_011535119.1:c.2336G=
|
XP_011533421.1:p.Trp779=
|
|
|
XM_011535120.1:c.1922G=
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|
|
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XM_011535121.1:c.2336G=
|
XP_011533423.1:p.Trp779=
|
|
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XM_011535122.1:c.1004G=
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|
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XR_941601.1:n.2555G=
|
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XR_941602.1:n.2555G=
|
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XR_941603.1:n.2555G=
|
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XR_941604.1:n.2555G=
|
|
|
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NM_001330578.1:c.2122-723G=
|
NP_001317507.1:n.2122-723G=
|
|
|
NM_001330579.1:c.2084G=
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NP_001317508.1:p.Trp695=
|
|
|
XM_005266424.4:c.2240G=
|
XP_005266481.1:p.Trp747=
|
|
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XM_005266430.4:c.2336G=
|
XP_005266487.1:p.Trp779=
|
|
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XM_005266431.4:c.2300G=
|
XP_005266488.1:p.Trp767=
|
|
|
XM_006719837.3:c.2240G=
|
XP_006719900.1:p.Trp747=
|
|
|
XM_011535117.3:c.2240G=
|
XP_011533419.1:p.Trp747=
|
|
|
XM_017020627.1:c.2240G=
|
XP_016876116.1:p.Trp747=
|
|
|
NM_000053.4:c.2336G=
MANE Select
|
NP_000044.2:p.Trp779=
|
|
|
NM_001005918.3:c.1870-723G=
|
NP_001005918.1:n.1870-723G=
|
|
|
NM_001330579.2:c.2084G=
|
NP_001317508.1:p.Trp695=
|
|
|
NM_001243182.2:c.2003G=
|
NP_001230111.1:p.Trp668=
|
|
|
NM_001330578.2:c.2122-723G=
|
NP_001317507.1:n.2122-723G=
|
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