ENST00000295897.9:c.446C>G
MANE Select
|
ENSP00000295897.4:p.Thr149Ser
|
|
ENST00000295897.8:c.446C>G
|
ENSP00000295897.4:p.Thr149Ser
|
|
ENST00000401494.7:c.138-586C>G
|
ENSP00000384695.3:n.138-586C>G
|
|
ENST00000415165.6:c.138-3227C>G
|
ENSP00000401820.2:n.138-3227C>G
|
|
ENST00000441319.5:c.452C>G
|
ENSP00000392541.1:p.Thr151Ser
|
|
ENST00000476441.6:c.80-586C>G
|
ENSP00000423727.1:n.80-586C>G
|
|
ENST00000503124.5:c.33-586C>G
|
ENSP00000421027.1:n.33-586C>G
|
|
ENST00000505649.5:n.132C>G
|
|
|
ENST00000509063.5:c.446C>G
|
ENSP00000422784.1:p.Thr149Ser
|
|
ENST00000510166.5:n.482C>G
|
|
|
ENST00000514786.1:n.415C>G
|
|
|
ENST00000515133.5:n.487C>G
|
|
|
ENST00000621085.4:c.446C>G
|
ENSP00000483421.1:p.Thr149Ser
|
|
ENST00000621628.4:c.446C>G
|
ENSP00000480485.1:p.Thr149Ser
|
|
NM_000477.5:c.446C>G
|
NP_000468.1:p.Thr149Ser
|
|
NM_000477.6:c.446C>G
|
NP_000468.1:p.Thr149Ser
|
|
NM_000477.7:c.446C>G
MANE Select
|
NP_000468.1:p.Thr149Ser
|
|