|
ENST00000375687.10:c.3863G>C
MANE Select
|
ENSP00000364839.4:p.Gly1288Ala
|
|
|
ENST00000646985.1:c.3680G>C
|
ENSP00000495053.1:p.Gly1227Ala
|
|
|
ENST00000647223.1:n.6216G>C
|
|
|
|
ENST00000651418.1:c.1870-1855G>C
|
ENSP00000499150.1:n.1870-1855G>C
|
|
|
ENST00000306058.9:c.3848G>C
|
ENSP00000305119.5:p.Gly1283Ala
|
|
|
ENST00000375687.8:c.3863G>C
|
ENSP00000364839.4:p.Gly1288Ala
|
|
|
ENST00000613218.4:c.3863G>C
|
ENSP00000480487.1:p.Gly1288Ala
|
|
|
ENST00000620121.4:c.3863G>C
|
ENSP00000481978.1:p.Gly1288Ala
|
|
|
NM_015338.5:c.3863G>C , LRG_630t1:c.3863G>C
|
NP_056153.2:p.Gly1288Ala
|
|
|
XM_006723727.2:c.3860G>C
|
XP_006723790.1:p.Gly1287Ala
|
|
|
XM_006723728.2:c.3833G>C
|
XP_006723791.1:p.Gly1278Ala
|
|
|
XM_006723730.2:c.3779G>C
|
XP_006723793.1:p.Gly1260Ala
|
|
|
XM_006723732.2:c.3680G>C
|
XP_006723795.1:p.Gly1227Ala
|
|
|
XM_006723733.1:c.3179G>C
|
XP_006723796.1:p.Gly1060Ala
|
|
|
XM_011528647.1:c.4127G>C
|
XP_011526949.1:p.Gly1376Ala
|
|
|
XM_011528648.1:c.4124G>C
|
XP_011526950.1:p.Gly1375Ala
|
|
|
XM_011528649.1:c.4043G>C
|
XP_011526951.1:p.Gly1348Ala
|
|
|
XM_011528650.1:c.3974G>C
|
XP_011526952.1:p.Gly1325Ala
|
|
|
XM_011528651.1:c.3842G>C
|
XP_011526953.1:p.Gly1281Ala
|
|
|
XM_011528652.1:c.3779G>C
|
XP_011526954.1:p.Gly1260Ala
|
|
|
NM_001363734.1:c.3680G>C
|
NP_001350663.1:p.Gly1227Ala
|
|
|
XM_006723727.3:c.3860G>C
|
XP_006723790.1:p.Gly1287Ala
|
|
|
XM_006723728.3:c.3833G>C
|
XP_006723791.1:p.Gly1278Ala
|
|
|
XM_006723730.4:c.3779G>C
|
XP_006723793.1:p.Gly1260Ala
|
|
|
XM_011528648.3:c.4124G>C
|
XP_011526950.1:p.Gly1375Ala
|
|
|
XM_011528652.2:c.3779G>C
|
XP_011526954.1:p.Gly1260Ala
|
|
|
XM_017027704.1:c.3779G>C
|
XP_016883193.1:p.Gly1260Ala
|
|
|
XM_017027705.1:c.3779G>C
|
XP_016883194.1:p.Gly1260Ala
|
|
|
XM_017027706.1:c.3710G>C
|
XP_016883195.1:p.Gly1237Ala
|
|
|
NM_015338.6:c.3863G>C
MANE Select
|
NP_056153.2:p.Gly1288Ala
|
|
