ENST00000704002.1:c.569G>A
|
ENSP00000515615.1:p.Cys190Tyr
|
|
ENST00000704003.1:c.*423G>A
|
ENSP00000515616.1:n.*423G>A
|
|
ENST00000348035.9:c.470G>A
MANE Select
|
ENSP00000258737.7:p.Cys157Tyr
|
|
ENST00000348035.8:c.470G>A
|
ENSP00000258737.7:p.Cys157Tyr
|
|
ENST00000356142.4:c.527G>A
|
ENSP00000348461.4:p.Cys176Tyr
|
|
ENST00000473564.1:n.548G>A
|
|
|
ENST00000488373.5:n.701G>A
|
|
|
ENST00000495499.1:n.432G>A
|
|
|
ENST00000497741.5:n.486G>A
|
|
|
NM_006908.4:c.470G>A
|
NP_008839.2:p.Cys157Tyr
|
|
NM_018890.3:c.527G>A
|
NP_061485.1:p.Cys176Tyr
|
|
NM_006908.5:c.470G>A
MANE Select
|
NP_008839.2:p.Cys157Tyr
|
|
NM_018890.4:c.527G>A
|
NP_061485.1:p.Cys176Tyr
|
|