|
ENST00000375687.10:c.3724G>T
MANE Select
|
ENSP00000364839.4:p.Asp1242Tyr
|
|
|
ENST00000646985.1:c.3541G>T
|
ENSP00000495053.1:p.Asp1181Tyr
|
|
|
ENST00000647223.1:n.6077G>T
|
|
|
|
ENST00000651418.1:c.1869+1855G>T
|
ENSP00000499150.1:n.1869+1855G>T
|
|
|
ENST00000306058.9:c.3709G>T
|
ENSP00000305119.5:p.Asp1237Tyr
|
|
|
ENST00000375687.8:c.3724G>T
|
ENSP00000364839.4:p.Asp1242Tyr
|
|
|
ENST00000613218.4:c.3724G>T
|
ENSP00000480487.1:p.Asp1242Tyr
|
|
|
ENST00000620121.4:c.3724G>T
|
ENSP00000481978.1:p.Asp1242Tyr
|
|
|
NM_015338.5:c.3724G>T , LRG_630t1:c.3724G>T
|
NP_056153.2:p.Asp1242Tyr
|
|
|
XM_006723727.2:c.3721G>T
|
XP_006723790.1:p.Asp1241Tyr
|
|
|
XM_006723728.2:c.3694G>T
|
XP_006723791.1:p.Asp1232Tyr
|
|
|
XM_006723730.2:c.3640G>T
|
XP_006723793.1:p.Asp1214Tyr
|
|
|
XM_006723732.2:c.3541G>T
|
XP_006723795.1:p.Asp1181Tyr
|
|
|
XM_006723733.1:c.3040G>T
|
XP_006723796.1:p.Asp1014Tyr
|
|
|
XM_011528647.1:c.3988G>T
|
XP_011526949.1:p.Asp1330Tyr
|
|
|
XM_011528648.1:c.3985G>T
|
XP_011526950.1:p.Asp1329Tyr
|
|
|
XM_011528649.1:c.3904G>T
|
XP_011526951.1:p.Asp1302Tyr
|
|
|
XM_011528650.1:c.3835G>T
|
XP_011526952.1:p.Asp1279Tyr
|
|
|
XM_011528651.1:c.3703G>T
|
XP_011526953.1:p.Asp1235Tyr
|
|
|
XM_011528652.1:c.3640G>T
|
XP_011526954.1:p.Asp1214Tyr
|
|
|
NM_001363734.1:c.3541G>T
|
NP_001350663.1:p.Asp1181Tyr
|
|
|
XM_006723727.3:c.3721G>T
|
XP_006723790.1:p.Asp1241Tyr
|
|
|
XM_006723728.3:c.3694G>T
|
XP_006723791.1:p.Asp1232Tyr
|
|
|
XM_006723730.4:c.3640G>T
|
XP_006723793.1:p.Asp1214Tyr
|
|
|
XM_011528648.3:c.3985G>T
|
XP_011526950.1:p.Asp1329Tyr
|
|
|
XM_011528652.2:c.3640G>T
|
XP_011526954.1:p.Asp1214Tyr
|
|
|
XM_017027704.1:c.3640G>T
|
XP_016883193.1:p.Asp1214Tyr
|
|
|
XM_017027705.1:c.3640G>T
|
XP_016883194.1:p.Asp1214Tyr
|
|
|
XM_017027706.1:c.3571G>T
|
XP_016883195.1:p.Asp1191Tyr
|
|
|
NM_015338.6:c.3724G>T
MANE Select
|
NP_056153.2:p.Asp1242Tyr
|
|
