|
ENST00000252444.10:c.2692A>T
|
ENSP00000252444.6:p.Asn898Tyr
|
|
|
ENST00000559340.2:c.*503A>T
|
ENSP00000453696.2:n.*503A>T
|
|
|
ENST00000560467.2:c.2314A>T
|
ENSP00000453513.2:p.Asn772Tyr
|
|
|
ENST00000558518.6:c.2434A>T
MANE Select
|
ENSP00000454071.1:p.Asn812Tyr
|
|
|
ENST00000252444.9:c.2688A>T
|
|
|
|
ENST00000455727.6:c.1930A>T
|
ENSP00000397829.2:p.Asn644Tyr
|
|
|
ENST00000535915.5:c.2311A>T
|
ENSP00000440520.1:p.Asn771Tyr
|
|
|
ENST00000545707.5:c.1900A>T
|
ENSP00000437639.1:p.Asn634Tyr
|
|
|
ENST00000557933.5:c.2496A>T
|
ENSP00000453557.1:p.Arg832Ser
|
|
|
ENST00000558013.5:c.2434A>T
|
ENSP00000453346.1:p.Asn812Tyr
|
|
|
ENST00000558518.5:c.2434A>T
|
ENSP00000454071.1:p.Asn812Tyr
|
|
|
ENST00000560628.1:n.108+1903A>T
|
|
|
|
NM_000527.4:c.2434A>T , LRG_274t1:c.2434A>T
|
NP_000518.1:p.Asn812Tyr
|
|
|
NM_001195798.1:c.2434A>T
|
NP_001182727.1:p.Asn812Tyr
|
|
|
NM_001195799.1:c.2311A>T
|
NP_001182728.1:p.Asn771Tyr
|
|
|
NM_001195800.1:c.1930A>T
|
NP_001182729.1:p.Asn644Tyr
|
|
|
NM_001195803.1:c.1900A>T
|
NP_001182732.1:p.Asn634Tyr
|
|
|
XM_011528010.1:c.2356A>T
|
XP_011526312.1:p.Asn786Tyr
|
|
|
XM_011528011.1:c.2053A>T
|
XP_011526313.1:p.Asn685Tyr
|
|
|
XR_244074.2:n.2444A>T
|
|
|
|
XM_011528010.2:c.2356A>T
|
XP_011526312.1:p.Asn786Tyr
|
|
|
XR_001753685.2:n.2768A>T
|
|
|
|
XR_001753686.2:n.2411A>T
|
|
|
|
NM_000527.5:c.2434A>T
MANE Select
|
NP_000518.1:p.Asn812Tyr
|
|
|
NM_001195798.2:c.2434A>T
|
NP_001182727.1:p.Asn812Tyr
|
|
|
NM_001195799.2:c.2311A>T
|
NP_001182728.1:p.Asn771Tyr
|
|
|
NM_001195800.2:c.1930A>T
|
NP_001182729.1:p.Asn644Tyr
|
|
|
NM_001195803.2:c.1900A>T
|
NP_001182732.1:p.Asn634Tyr
|
|
