ENST00000400521.7:c.1171G>T
MANE Select
|
ENSP00000383365.1:p.Asp391Tyr
|
|
ENST00000400518.5:c.1081G>T
|
ENSP00000383362.1:p.Asp361Tyr
|
|
ENST00000400519.6:c.1168G>T
|
ENSP00000383363.1:p.Asp390Tyr
|
|
ENST00000400521.6:c.1171G>T
|
ENSP00000383365.1:p.Asp391Tyr
|
|
ENST00000400525.6:c.1102G>T
|
ENSP00000383369.3:p.Asp368Tyr
|
|
ENST00000462330.5:c.94G>T
|
ENSP00000485603.2:p.Asp32Tyr
|
|
ENST00000462843.2:c.121G>T
|
ENSP00000485466.2:p.Asp41Tyr
|
|
ENST00000474308.5:c.1114G>T
|
ENSP00000485665.1:p.Asp372Tyr
|
|
ENST00000485358.5:c.139G>T
|
ENSP00000485499.2:p.Asp47Tyr
|
|
ENST00000487165.5:n.1265G>T
|
|
|
ENST00000494454.5:n.1245G>T
|
|
|
ENST00000495655.2:n.715G>T
|
|
|
ENST00000542719.6:c.883G>T
|
ENSP00000485128.2:p.Asp295Tyr
|
|
ENST00000634471.1:n.244-362G>T
|
|
|
ENST00000634537.1:c.400G>T
|
ENSP00000489208.1:p.Asp134Tyr
|
|
NM_006440.4:c.1171G>T
|
NP_006431.2:p.Asp391Tyr
|
|
NM_001352300.1:c.1168G>T
|
NP_001339229.1:p.Asp390Tyr
|
|
NM_001352301.1:c.1081G>T
|
NP_001339230.1:p.Asp361Tyr
|
|
NM_001352302.1:c.883G>T
|
NP_001339231.1:p.Asp295Tyr
|
|
NR_147957.1:n.1303G>T
|
|
|
NM_006440.5:c.1171G>T
MANE Select
|
NP_006431.2:p.Asp391Tyr
|
|
NM_001352300.2:c.1168G>T
|
NP_001339229.1:p.Asp390Tyr
|
|
NR_147957.2:n.1129G>T
|
|
|
NM_001352301.2:c.1081G>T
|
NP_001339230.1:p.Asp361Tyr
|
|
NM_001352302.2:c.883G>T
|
NP_001339231.1:p.Asp295Tyr
|
|