ENST00000265104.5:c.10726T>G
MANE Select
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ENSP00000265104.4:p.Trp3576Gly
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ENST00000681290.1:c.10681T>G
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ENSP00000505288.1:p.Trp3561Gly
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ENST00000265104.4:c.10726T>G
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ENSP00000265104.4:p.Trp3576Gly
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NM_001369.2:c.10726T>G
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NP_001360.1:p.Trp3576Gly
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XM_005248262.2:c.10681T>G
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XP_005248319.1:p.Trp3561Gly
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XM_005248262.3:c.10834T>G
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XP_005248319.2:p.Trp3612Gly
|
|
XM_017009177.1:c.10834T>G
|
XP_016864666.1:p.Trp3612Gly
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XM_017009178.1:c.9739T>G
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XP_016864667.1:p.Trp3247Gly
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XM_017009179.2:c.9739T>G
|
XP_016864668.1:p.Trp3247Gly
|
|
XM_017009180.1:c.10834T>G
|
XP_016864669.1:p.Trp3612Gly
|
|
XM_017009181.1:c.10834T>G
|
XP_016864670.1:p.Trp3612Gly
|
|
XM_017009182.1:c.10834T>G
|
XP_016864671.1:p.Trp3612Gly
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|
XM_017009185.1:c.5923T>G
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XP_016864674.1:p.Trp1975Gly
|
|
XM_017009186.1:c.5476T>G
|
XP_016864675.1:p.Trp1826Gly
|
|
XM_017009188.1:c.4813T>G
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XP_016864677.1:p.Trp1605Gly
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XM_024454388.1:c.9739T>G
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XP_024310156.1:p.Trp3247Gly
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|
XM_024454389.1:c.9328T>G
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XP_024310157.1:p.Trp3110Gly
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NM_001369.3:c.10726T>G
MANE Select
|
NP_001360.1:p.Trp3576Gly
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