ENST00000295897.9:c.213T>C
MANE Select
|
ENSP00000295897.4:p.Thr71=
|
|
ENST00000295897.8:c.213T>C
|
ENSP00000295897.4:p.Thr71=
|
|
ENST00000401494.7:c.137+1531T>C
|
ENSP00000384695.3:n.137+1531T>C
|
|
ENST00000415165.6:c.137+1531T>C
|
ENSP00000401820.2:n.137+1531T>C
|
|
ENST00000441319.5:c.219T>C
|
ENSP00000392541.1:p.Thr73=
|
|
ENST00000476441.6:c.79+2298T>C
|
ENSP00000423727.1:n.79+2298T>C
|
|
ENST00000503124.5:c.-26T>C
|
ENSP00000421027.1:n.-26T>C
|
|
ENST00000509063.5:c.213T>C
|
ENSP00000422784.1:p.Thr71=
|
|
ENST00000510166.5:n.249T>C
|
|
|
ENST00000514786.1:n.182T>C
|
|
|
ENST00000515133.5:n.254T>C
|
|
|
ENST00000621085.4:c.213T>C
|
ENSP00000483421.1:p.Thr71=
|
|
ENST00000621628.4:c.213T>C
|
ENSP00000480485.1:p.Thr71=
|
|
NM_000477.5:c.213T>C
|
NP_000468.1:p.Thr71=
|
|
NM_000477.6:c.213T>C
|
NP_000468.1:p.Thr71=
|
|
NM_000477.7:c.213T>C
MANE Select
|
NP_000468.1:p.Thr71=
|
|