ENST00000398603.6:c.337-166G=
|
ENSP00000381604.1:n.337-166G=
|
|
ENST00000398606.10:c.444+12G=
MANE Select
|
ENSP00000381607.3:n.444+12G=
|
|
ENST00000646888.1:c.*160+12G=
|
ENSP00000494477.1:n.*160+12G=
|
|
ENST00000398603.5:c.337-166G=
|
ENSP00000381604.1:n.337-166G=
|
|
ENST00000398606.7:c.444+12G=
|
ENSP00000381607.3:n.444+12G=
|
|
ENST00000467591.1:n.555+12G=
|
|
|
ENST00000494593.1:n.1251G=
|
|
|
ENST00000495996.1:c.120G=
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ENSP00000484686.1:p.Trp40=
|
|
ENST00000498765.5:c.507+12G=
|
|
|
NM_000852.3:c.444+12G= , LRG_723t1:c.444+12G=
|
NP_000843.1:n.444+12G=
|
|
NM_000852.4:c.444+12G=
MANE Select
|
NP_000843.1:n.444+12G=
|
|