ENST00000696049.1:c.507+39A=
|
ENSP00000512353.1:n.507+39A=
|
|
ENST00000696479.1:c.618A=
|
ENSP00000512655.1:p.Thr206=
|
|
ENST00000427473.3:n.491+533A=
|
|
|
ENST00000648405.2:c.546A=
MANE Select
|
ENSP00000497102.1:p.Thr182=
|
|
ENST00000650075.1:n.570A=
|
|
|
ENST00000295854.10:c.457+533A=
|
ENSP00000295854.6:n.457+533A=
|
|
ENST00000302823.7:c.546A=
|
ENSP00000303939.3:p.Thr182=
|
|
ENST00000427473.2:c.346+533A=
|
ENSP00000409707.2:n.346+533A=
|
|
ENST00000472206.1:c.172+818A=
|
ENSP00000417779.1:n.172+818A=
|
|
ENST00000487393.1:n.110-1242A=
|
|
|
NM_001037631.2:c.457+533A=
|
NP_001032720.1:n.457+533A=
|
|
NM_005214.4:c.546A=
|
NP_005205.2:p.Thr182=
|
|
XR_241294.1:n.686A=
|
|
|
NM_001037631.3:c.457+533A=
|
NP_001032720.1:n.457+533A=
|
|
NM_005214.5:c.546A=
MANE Select
|
NP_005205.2:p.Thr182=
|
|