ENST00000339818.9:c.346C>G
MANE Select
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ENSP00000344566.4:p.Pro116Ala
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ENST00000325223.7:c.346C>G
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ENSP00000317302.7:p.Pro116Ala
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ENST00000339818.8:c.346C>G
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ENSP00000344566.4:p.Pro116Ala
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ENST00000397956.7:c.346C>G
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ENSP00000381047.3:p.Pro116Ala
|
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ENST00000462742.1:n.2517C>G
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ENST00000478674.1:n.405C>G
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|
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ENST00000496321.5:n.462C>G
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|
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NM_001271440.1:c.346C>G
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NP_001258369.1:p.Pro116Ala
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NM_001271441.1:c.346C>G
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NP_001258370.1:p.Pro116Ala
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NM_001271442.1:c.223C>G
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NP_001258371.1:p.Pro75Ala
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NM_004928.2:c.346C>G
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NP_004919.1:p.Pro116Ala
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XM_006724051.2:c.421C>G
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XP_006724114.1:p.Pro141Ala
|
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XM_006724052.2:c.421C>G
|
XP_006724115.1:p.Pro141Ala
|
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XM_006724053.2:c.22C>G
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XP_006724116.1:p.Pro8Ala
|
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XR_937571.1:n.549C>G
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|
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XM_006724051.3:c.421C>G
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XP_006724114.1:p.Pro141Ala
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XM_006724053.3:c.22C>G
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XP_006724116.1:p.Pro8Ala
|
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XM_017028470.1:c.550C>G
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XP_016883959.1:p.Pro184Ala
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XM_017028471.1:c.295C>G
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XP_016883960.1:p.Pro99Ala
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XM_017028472.1:c.22C>G
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XP_016883961.1:p.Pro8Ala
|
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XR_937571.2:n.556C>G
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|
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NM_004928.3:c.346C>G
MANE Select
|
NP_004919.1:p.Pro116Ala
|
|
NM_001271440.2:c.346C>G
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NP_001258369.1:p.Pro116Ala
|
|
NM_001271441.2:c.346C>G
|
NP_001258370.1:p.Pro116Ala
|
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