ENST00000422447.8:c.997T>G
MANE Select
|
ENSP00000395337.3:p.Ter333Glu
|
|
ENST00000227157.8:c.*147T>G
|
ENSP00000227157.4:n.*147T>G
|
|
ENST00000375710.7:n.1864T>G
|
|
|
ENST00000379412.9:c.997T>G
|
ENSP00000368722.5:p.Ter333Glu
|
|
ENST00000396222.6:c.728T>G
|
ENSP00000379524.2:p.Leu243Ter
|
|
ENST00000422447.7:c.997T>G
|
ENSP00000395337.3:p.Ter333Glu
|
|
ENST00000430553.6:c.823T>G
|
ENSP00000406172.2:p.Ter275Glu
|
|
ENST00000538451.1:n.884T>G
|
|
|
ENST00000540430.5:c.1084T>G
|
ENSP00000445175.1:p.Ter362Glu
|
|
ENST00000542179.1:c.997T>G
|
ENSP00000445331.1:p.Ter333Glu
|
|
ENST00000545215.5:c.*741T>G
|
ENSP00000442637.1:n.*741T>G
|
|
NM_001135239.1:c.823T>G
|
NP_001128711.1:p.Ter275Glu
|
|
NM_001165414.1:c.1084T>G
|
NP_001158886.1:p.Ter362Glu
|
|
NM_001165415.1:c.728T>G
|
NP_001158887.1:p.Leu243Ter
|
|
NM_001165416.1:c.*147T>G
|
NP_001158888.1:n.*147T>G
|
|
NM_005566.3:c.997T>G
|
NP_005557.1:p.Ter333Glu
|
|
NR_028500.1:n.1151T>G
|
|
|
NM_005566.4:c.997T>G
MANE Select
|
NP_005557.1:p.Ter333Glu
|
|
NM_001165415.2:c.728T>G
|
NP_001158887.1:p.Leu243Ter
|
|
NM_001135239.2:c.823T>G
|
NP_001128711.1:p.Ter275Glu
|
|
NM_001165414.2:c.1084T>G
|
NP_001158886.1:p.Ter362Glu
|
|
NM_001165416.2:c.*147T>G
|
NP_001158888.1:n.*147T>G
|
|
NR_028500.2:n.977T>G
|
|
|