ENST00000265104.5:c.9471T>G
MANE Select
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ENSP00000265104.4:p.Ala3157=
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ENST00000681290.1:c.9426T>G
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ENSP00000505288.1:p.Ala3142=
|
|
ENST00000265104.4:c.9471T>G
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ENSP00000265104.4:p.Ala3157=
|
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ENST00000504001.3:n.183T>G
|
|
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NM_001369.2:c.9471T>G
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NP_001360.1:p.Ala3157=
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|
XM_005248262.2:c.9426T>G
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XP_005248319.1:p.Ala3142=
|
|
XM_005248262.3:c.9579T>G
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XP_005248319.2:p.Ala3193=
|
|
XM_017009177.1:c.9579T>G
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XP_016864666.1:p.Ala3193=
|
|
XM_017009178.1:c.8484T>G
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XP_016864667.1:p.Ala2828=
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|
XM_017009179.2:c.8484T>G
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XP_016864668.1:p.Ala2828=
|
|
XM_017009180.1:c.9579T>G
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XP_016864669.1:p.Ala3193=
|
|
XM_017009181.1:c.9579T>G
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XP_016864670.1:p.Ala3193=
|
|
XM_017009182.1:c.9579T>G
|
XP_016864671.1:p.Ala3193=
|
|
XM_017009183.1:c.9579T>G
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XP_016864672.1:p.Ala3193=
|
|
XM_017009185.1:c.4668T>G
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XP_016864674.1:p.Ala1556=
|
|
XM_017009186.1:c.4221T>G
|
XP_016864675.1:p.Ala1407=
|
|
XM_017009188.1:c.3558T>G
|
XP_016864677.1:p.Ala1186=
|
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XM_024454388.1:c.8484T>G
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XP_024310156.1:p.Ala2828=
|
|
XM_024454389.1:c.8073T>G
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XP_024310157.1:p.Ala2691=
|
|
NM_001369.3:c.9471T>G
MANE Select
|
NP_001360.1:p.Ala3157=
|
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