ENST00000379370.7:c.3897C>G
MANE Select
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ENSP00000368678.2:p.Ala1299=
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ENST00000651234.1:c.3582C>G
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ENSP00000499046.1:p.Ala1194=
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ENST00000652369.1:c.3582C>G
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ENSP00000498543.1:p.Ala1194=
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ENST00000379370.6:c.3897C>G
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ENSP00000368678.2:p.Ala1299=
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ENST00000620552.4:c.3483C>G
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ENSP00000484607.1:p.Ala1161=
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NM_001305275.1:c.3897C>G
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NP_001292204.1:p.Ala1299=
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NM_198576.3:c.3897C>G
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NP_940978.2:p.Ala1299=
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XM_005244749.2:c.3897C>G
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XP_005244806.1:p.Ala1299=
|
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XM_006710635.2:c.3897C>G
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XP_006710698.1:p.Ala1299=
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XM_011541429.1:c.3897C>G
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XP_011539731.1:p.Ala1299=
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XM_011541430.1:c.3024C>G
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XP_011539732.1:p.Ala1008=
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XM_011541431.1:c.2163C>G
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XP_011539733.1:p.Ala721=
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XR_946650.1:n.3964C>G
|
|
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NM_001364727.1:c.3582C>G
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NP_001351656.1:p.Ala1194=
|
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XM_005244749.3:c.3897C>G
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XP_005244806.1:p.Ala1299=
|
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XM_011541429.2:c.3897C>G
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XP_011539731.1:p.Ala1299=
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XR_946650.2:n.3968C>G
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|
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NM_001305275.2:c.3897C>G
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NP_001292204.1:p.Ala1299=
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NM_198576.4:c.3897C>G
MANE Select
|
NP_940978.2:p.Ala1299=
|
|
NM_001364727.2:c.3582C>G
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NP_001351656.1:p.Ala1194=
|
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