ENST00000696049.1:c.497T>C
|
ENSP00000512353.1:p.Ile166Thr
|
|
ENST00000696479.1:c.569T>C
|
ENSP00000512655.1:p.Ile190Thr
|
|
ENST00000427473.3:n.491+484T>C
|
|
|
ENST00000648405.2:c.497T>C
MANE Select
|
ENSP00000497102.1:p.Ile166Thr
|
|
ENST00000650075.1:n.521T>C
|
|
|
ENST00000295854.10:c.457+484T>C
|
ENSP00000295854.6:n.457+484T>C
|
|
ENST00000302823.7:c.497T>C
|
ENSP00000303939.3:p.Ile166Thr
|
|
ENST00000427473.2:c.346+484T>C
|
ENSP00000409707.2:n.346+484T>C
|
|
ENST00000472206.1:c.172+769T>C
|
ENSP00000417779.1:n.172+769T>C
|
|
ENST00000487393.1:n.110-1291T>C
|
|
|
NM_001037631.2:c.457+484T>C
|
NP_001032720.1:n.457+484T>C
|
|
NM_005214.4:c.497T>C
|
NP_005205.2:p.Ile166Thr
|
|
XR_241294.1:n.637T>C
|
|
|
NM_001037631.3:c.457+484T>C
|
NP_001032720.1:n.457+484T>C
|
|
NM_005214.5:c.497T>C
MANE Select
|
NP_005205.2:p.Ile166Thr
|
|