ENST00000696049.1:c.504A>T
|
ENSP00000512353.1:p.Ala168=
|
|
ENST00000696479.1:c.576A>T
|
ENSP00000512655.1:p.Ala192=
|
|
ENST00000427473.3:n.491+491A>T
|
|
|
ENST00000648405.2:c.504A>T
MANE Select
|
ENSP00000497102.1:p.Ala168=
|
|
ENST00000650075.1:n.528A>T
|
|
|
ENST00000295854.10:c.457+491A>T
|
ENSP00000295854.6:n.457+491A>T
|
|
ENST00000302823.7:c.504A>T
|
ENSP00000303939.3:p.Ala168=
|
|
ENST00000427473.2:c.346+491A>T
|
ENSP00000409707.2:n.346+491A>T
|
|
ENST00000472206.1:c.172+776A>T
|
ENSP00000417779.1:n.172+776A>T
|
|
ENST00000487393.1:n.110-1284A>T
|
|
|
NM_001037631.2:c.457+491A>T
|
NP_001032720.1:n.457+491A>T
|
|
NM_005214.4:c.504A>T
|
NP_005205.2:p.Ala168=
|
|
XR_241294.1:n.644A>T
|
|
|
NM_001037631.3:c.457+491A>T
|
NP_001032720.1:n.457+491A>T
|
|
NM_005214.5:c.504A>T
MANE Select
|
NP_005205.2:p.Ala168=
|
|