ENST00000295897.9:c.1595C>T
MANE Select
|
ENSP00000295897.4:p.Thr532Ile
|
|
ENST00000295897.8:c.1595C>T
|
ENSP00000295897.4:p.Thr532Ile
|
|
ENST00000401494.7:c.1250C>T
|
ENSP00000384695.3:p.Thr417Ile
|
|
ENST00000415165.6:c.1019C>T
|
ENSP00000401820.2:p.Thr340Ile
|
|
ENST00000476441.6:c.*874C>T
|
ENSP00000423727.1:n.*874C>T
|
|
ENST00000486939.1:n.249C>T
|
|
|
ENST00000503124.5:c.1145C>T
|
ENSP00000421027.1:p.Thr382Ile
|
|
ENST00000505649.5:n.1142C>T
|
|
|
ENST00000509063.5:c.1595C>T
|
ENSP00000422784.1:p.Thr532Ile
|
|
ENST00000511370.1:c.1128C>T
|
|
|
ENST00000621085.4:c.956C>T
|
ENSP00000483421.1:p.Thr319Ile
|
|
ENST00000621628.4:c.956C>T
|
ENSP00000480485.1:p.Thr319Ile
|
|
NM_000477.5:c.1595C>T
|
NP_000468.1:p.Thr532Ile
|
|
NM_000477.6:c.1595C>T
|
NP_000468.1:p.Thr532Ile
|
|
NM_000477.7:c.1595C>T
MANE Select
|
NP_000468.1:p.Thr532Ile
|
|