|
ENST00000252444.10:c.2670G>C
|
ENSP00000252444.6:p.Leu890=
|
|
|
ENST00000559340.2:c.*481G>C
|
ENSP00000453696.2:n.*481G>C
|
|
|
ENST00000560467.2:c.2292G>C
|
ENSP00000453513.2:p.Leu764=
|
|
|
ENST00000558518.6:c.2412G>C
MANE Select
|
ENSP00000454071.1:p.Leu804=
|
|
|
ENST00000252444.9:c.2666G>C
|
|
|
|
ENST00000455727.6:c.1908G>C
|
ENSP00000397829.2:p.Leu636=
|
|
|
ENST00000535915.5:c.2289G>C
|
ENSP00000440520.1:p.Leu763=
|
|
|
ENST00000545707.5:c.1878G>C
|
ENSP00000437639.1:p.Leu626=
|
|
|
ENST00000557933.5:c.2474G>C
|
ENSP00000453557.1:p.Trp825Ser
|
|
|
ENST00000558013.5:c.2412G>C
|
ENSP00000453346.1:p.Leu804=
|
|
|
ENST00000558518.5:c.2412G>C
|
ENSP00000454071.1:p.Leu804=
|
|
|
ENST00000560628.1:n.108+1881G>C
|
|
|
|
NM_000527.4:c.2412G>C , LRG_274t1:c.2412G>C
|
NP_000518.1:p.Leu804=
|
|
|
NM_001195798.1:c.2412G>C
|
NP_001182727.1:p.Leu804=
|
|
|
NM_001195799.1:c.2289G>C
|
NP_001182728.1:p.Leu763=
|
|
|
NM_001195800.1:c.1908G>C
|
NP_001182729.1:p.Leu636=
|
|
|
NM_001195803.1:c.1878G>C
|
NP_001182732.1:p.Leu626=
|
|
|
XM_011528010.1:c.2334G>C
|
XP_011526312.1:p.Leu778=
|
|
|
XM_011528011.1:c.2031G>C
|
XP_011526313.1:p.Leu677=
|
|
|
XR_244074.2:n.2422G>C
|
|
|
|
XM_011528010.2:c.2334G>C
|
XP_011526312.1:p.Leu778=
|
|
|
XR_001753685.2:n.2746G>C
|
|
|
|
XR_001753686.2:n.2389G>C
|
|
|
|
NM_000527.5:c.2412G>C
MANE Select
|
NP_000518.1:p.Leu804=
|
|
|
NM_001195798.2:c.2412G>C
|
NP_001182727.1:p.Leu804=
|
|
|
NM_001195799.2:c.2289G>C
|
NP_001182728.1:p.Leu763=
|
|
|
NM_001195800.2:c.1908G>C
|
NP_001182729.1:p.Leu636=
|
|
|
NM_001195803.2:c.1878G>C
|
NP_001182732.1:p.Leu626=
|
|
