ENST00000339818.9:c.292C>G
MANE Select
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ENSP00000344566.4:p.Pro98Ala
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ENST00000325223.7:c.292C>G
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ENSP00000317302.7:p.Pro98Ala
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ENST00000339818.8:c.292C>G
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ENSP00000344566.4:p.Pro98Ala
|
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ENST00000397956.7:c.292C>G
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ENSP00000381047.3:p.Pro98Ala
|
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ENST00000462742.1:n.2463C>G
|
|
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ENST00000478674.1:n.351C>G
|
|
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ENST00000496321.5:n.408C>G
|
|
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NM_001271440.1:c.292C>G
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NP_001258369.1:p.Pro98Ala
|
|
NM_001271441.1:c.292C>G
|
NP_001258370.1:p.Pro98Ala
|
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NM_001271442.1:c.169C>G
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NP_001258371.1:p.Pro57Ala
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NM_004928.2:c.292C>G
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NP_004919.1:p.Pro98Ala
|
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XM_006724051.2:c.367C>G
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XP_006724114.1:p.Pro123Ala
|
|
XM_006724052.2:c.367C>G
|
XP_006724115.1:p.Pro123Ala
|
|
XM_006724053.2:c.-33C>G
|
XP_006724116.1:n.-33C>G
|
|
XR_937571.1:n.495C>G
|
|
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XM_006724051.3:c.367C>G
|
XP_006724114.1:p.Pro123Ala
|
|
XM_006724053.3:c.-33C>G
|
XP_006724116.1:n.-33C>G
|
|
XM_017028470.1:c.496C>G
|
XP_016883959.1:p.Pro166Ala
|
|
XM_017028471.1:c.241C>G
|
XP_016883960.1:p.Pro81Ala
|
|
XM_017028472.1:c.-33C>G
|
XP_016883961.1:n.-33C>G
|
|
XR_937571.2:n.502C>G
|
|
|
NM_004928.3:c.292C>G
MANE Select
|
NP_004919.1:p.Pro98Ala
|
|
NM_001271440.2:c.292C>G
|
NP_001258369.1:p.Pro98Ala
|
|
NM_001271441.2:c.292C>G
|
NP_001258370.1:p.Pro98Ala
|
|