ENST00000375687.10:c.3858G>T
MANE Select
|
ENSP00000364839.4:p.Gln1286His
|
|
ENST00000646985.1:c.3675G>T
|
ENSP00000495053.1:p.Gln1225His
|
|
ENST00000647223.1:n.6211G>T
|
|
|
ENST00000651418.1:c.1870-1860G>T
|
ENSP00000499150.1:n.1870-1860G>T
|
|
ENST00000306058.9:c.3843G>T
|
ENSP00000305119.5:p.Gln1281His
|
|
ENST00000375687.8:c.3858G>T
|
ENSP00000364839.4:p.Gln1286His
|
|
ENST00000613218.4:c.3858G>T
|
ENSP00000480487.1:p.Gln1286His
|
|
ENST00000620121.4:c.3858G>T
|
ENSP00000481978.1:p.Gln1286His
|
|
NM_015338.5:c.3858G>T , LRG_630t1:c.3858G>T
|
NP_056153.2:p.Gln1286His
|
|
XM_006723727.2:c.3855G>T
|
XP_006723790.1:p.Gln1285His
|
|
XM_006723728.2:c.3828G>T
|
XP_006723791.1:p.Gln1276His
|
|
XM_006723730.2:c.3774G>T
|
XP_006723793.1:p.Gln1258His
|
|
XM_006723732.2:c.3675G>T
|
XP_006723795.1:p.Gln1225His
|
|
XM_006723733.1:c.3174G>T
|
XP_006723796.1:p.Gln1058His
|
|
XM_011528647.1:c.4122G>T
|
XP_011526949.1:p.Gln1374His
|
|
XM_011528648.1:c.4119G>T
|
XP_011526950.1:p.Gln1373His
|
|
XM_011528649.1:c.4038G>T
|
XP_011526951.1:p.Gln1346His
|
|
XM_011528650.1:c.3969G>T
|
XP_011526952.1:p.Gln1323His
|
|
XM_011528651.1:c.3837G>T
|
XP_011526953.1:p.Gln1279His
|
|
XM_011528652.1:c.3774G>T
|
XP_011526954.1:p.Gln1258His
|
|
NM_001363734.1:c.3675G>T
|
NP_001350663.1:p.Gln1225His
|
|
XM_006723727.3:c.3855G>T
|
XP_006723790.1:p.Gln1285His
|
|
XM_006723728.3:c.3828G>T
|
XP_006723791.1:p.Gln1276His
|
|
XM_006723730.4:c.3774G>T
|
XP_006723793.1:p.Gln1258His
|
|
XM_011528648.3:c.4119G>T
|
XP_011526950.1:p.Gln1373His
|
|
XM_011528652.2:c.3774G>T
|
XP_011526954.1:p.Gln1258His
|
|
XM_017027704.1:c.3774G>T
|
XP_016883193.1:p.Gln1258His
|
|
XM_017027705.1:c.3774G>T
|
XP_016883194.1:p.Gln1258His
|
|
XM_017027706.1:c.3705G>T
|
XP_016883195.1:p.Gln1235His
|
|
NM_015338.6:c.3858G>T
MANE Select
|
NP_056153.2:p.Gln1286His
|
|