|
NM_004990.4:c.986C>A
MANE Select
|
NP_004981.2:p.Pro329His
|
|
ENST00000262027.10:c.986C>A
MANE Select
|
ENSP00000262027.5:p.Pro329His
|
|
NM_004990.3:c.986C>A
|
NP_004981.2:p.Pro329His
|
|
ENST00000262027.9:c.986C>A
|
ENSP00000262027.5:p.Pro329His
|
|
ENST00000447721.6:n.628C>A
|
|
|
ENST00000537638.6:c.986C>A
|
ENSP00000446168.2:p.Pro329His
|
|
ENST00000545888.6:c.*487C>A
|
ENSP00000439307.2:n.*487C>A
|
|
ENST00000551892.1:c.*351C>A
|
ENSP00000450018.1:n.*351C>A
|
|
ENST00000552371.1:c.484C>A
|
|
|
ENST00000628866.2:c.*487C>A
|
ENSP00000486738.1:n.*487C>A
|
|
XM_006719398.2:c.284C>A
|
XP_006719461.1:p.Pro95His
|
|
XM_006719398.4:c.284C>A
|
XP_006719461.1:p.Pro95His
|
|
XM_011538353.1:c.986C>A
|
XP_011536655.1:p.Pro329His
|
|
XR_001748704.2:n.1009C>A
|
|
|
XR_002957327.1:n.933C>A
|
|