ENST00000696049.1:c.507+35T>A
|
ENSP00000512353.1:n.507+35T>A
|
|
ENST00000696479.1:c.614T>A
|
ENSP00000512655.1:p.Leu205His
|
|
ENST00000427473.3:n.491+529T>A
|
|
|
ENST00000648405.2:c.542T>A
MANE Select
|
ENSP00000497102.1:p.Leu181His
|
|
ENST00000650075.1:n.566T>A
|
|
|
ENST00000295854.10:c.457+529T>A
|
ENSP00000295854.6:n.457+529T>A
|
|
ENST00000302823.7:c.542T>A
|
ENSP00000303939.3:p.Leu181His
|
|
ENST00000427473.2:c.346+529T>A
|
ENSP00000409707.2:n.346+529T>A
|
|
ENST00000472206.1:c.172+814T>A
|
ENSP00000417779.1:n.172+814T>A
|
|
ENST00000487393.1:n.110-1246T>A
|
|
|
NM_001037631.2:c.457+529T>A
|
NP_001032720.1:n.457+529T>A
|
|
NM_005214.4:c.542T>A
|
NP_005205.2:p.Leu181His
|
|
XR_241294.1:n.682T>A
|
|
|
NM_001037631.3:c.457+529T>A
|
NP_001032720.1:n.457+529T>A
|
|
NM_005214.5:c.542T>A
MANE Select
|
NP_005205.2:p.Leu181His
|
|