ENST00000322213.9:c.3557T>A
MANE Select
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ENSP00000323421.3:p.Val1186Asp
|
|
ENST00000674590.1:c.2789T>A
|
ENSP00000502626.1:p.Val930Asp
|
|
ENST00000675504.1:c.3491T>A
|
ENSP00000502524.1:p.Val1164Asp
|
|
ENST00000322213.8:c.3557T>A
|
ENSP00000323421.3:p.Val1186Asp
|
|
ENST00000375340.10:c.3491T>A
|
ENSP00000364489.7:p.Val1164Asp
|
|
ENST00000470241.2:c.777T>A
|
|
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NM_001281463.1:c.3491T>A , LRG_773t1:c.3491T>A
|
NP_001268392.1:p.Val1164Asp
|
|
NM_006306.3:c.3557T>A , LRG_773t2:c.3557T>A
|
NP_006297.2:p.Val1186Asp
|
|
NM_006306.4:c.3557T>A
MANE Select
|
NP_006297.2:p.Val1186Asp
|
|