ENST00000372418.4:c.176G>C
|
ENSP00000361495.2:p.Gly59Ala
|
|
ENST00000372435.10:c.176G>C
MANE Select
|
ENSP00000361512.4:p.Gly59Ala
|
|
ENST00000643795.2:c.176G>C
|
ENSP00000496286.1:p.Gly59Ala
|
|
ENST00000644642.1:c.123-5829G>C
|
ENSP00000495493.1:n.123-5829G>C
|
|
ENST00000645638.1:c.*145G>C
|
ENSP00000496554.1:n.*145G>C
|
|
ENST00000645903.1:n.270G>C
|
|
|
ENST00000674525.1:n.261G>C
|
|
|
ENST00000674826.1:c.123-1554G>C
|
ENSP00000502278.1:n.123-1554G>C
|
|
ENST00000674843.1:c.278G>C
|
ENSP00000502260.1:n.278G>C
|
|
ENST00000675046.1:c.54G>C
|
|
|
ENST00000675304.1:n.109G>C
|
|
|
ENST00000675720.1:c.54G>C
|
|
|
ENST00000676092.1:c.176G>C
|
ENSP00000502780.1:p.Gly59Ala
|
|
ENST00000372419.3:c.176G>C
|
ENSP00000361496.3:p.Gly59Ala
|
|
ENST00000372428.8:c.-82-5829G>C
|
ENSP00000361505.5:n.-82-5829G>C
|
|
ENST00000372435.8:c.176G>C
|
ENSP00000361512.4:p.Gly59Ala
|
|
NM_001204402.1:c.-82-5829G>C
|
NP_001191331.1:n.-82-5829G>C
|
|
NM_002764.3:c.176G>C , LRG_264t1:c.176G>C
|
NP_002755.1:p.Gly59Ala
|
|
NM_002764.4:c.176G>C
MANE Select
|
NP_002755.1:p.Gly59Ala
|
|
NM_001204402.2:c.-82-5829G>C
|
NP_001191331.1:n.-82-5829G>C
|
|