ENST00000695870.1:n.1244G>A
|
|
|
ENST00000695872.1:n.128G>A
|
|
|
ENST00000695873.1:n.133G>A
|
|
|
ENST00000695874.1:n.265G>A
|
|
|
ENST00000695875.1:n.117G>A
|
|
|
ENST00000695876.1:n.87G>A
|
|
|
ENST00000328649.11:c.96G>A
MANE Select
|
ENSP00000333873.6:p.Arg32=
|
|
ENST00000650306.1:c.-454G>A
|
ENSP00000497451.1:n.-454G>A
|
|
ENST00000328649.10:c.96G>A
|
ENSP00000333873.6:p.Arg32=
|
|
ENST00000612800.1:c.216G>A
|
ENSP00000479860.1:p.Arg72=
|
|
NM_001277764.1:c.216G>A
|
NP_001264693.1:p.Arg72=
|
|
NM_006384.3:c.96G>A
|
NP_006375.2:p.Arg32=
|
|
NR_102427.1:n.282G>A
|
|
|
NR_102428.1:n.148G>A
|
|
|
XM_006720375.1:c.96G>A
|
XP_006720438.1:p.Arg32=
|
|
XM_006720375.2:c.96G>A
|
XP_006720438.1:p.Arg32=
|
|
NM_006384.4:c.96G>A
MANE Select
|
NP_006375.2:p.Arg32=
|
|
NM_001277764.2:c.216G>A
|
NP_001264693.1:p.Arg72=
|
|