ENST00000561514.3:c.3387T>G
|
ENSP00000460666.3:p.Cys1129Trp
|
|
ENST00000565038.2:c.*866T>G
|
ENSP00000459882.2:n.*866T>G
|
|
ENST00000566069.6:c.*16T>G
|
ENSP00000459237.2:n.*16T>G
|
|
ENST00000697377.2:c.3225T>G
|
ENSP00000513286.2:p.Cys1075Trp
|
|
ENST00000697379.2:c.3387T>G
|
ENSP00000513287.2:p.Cys1129Trp
|
|
ENST00000561514.2:c.2496T>G
|
ENSP00000460666.2:p.Cys832Trp
|
|
ENST00000697374.1:c.2496T>G
|
ENSP00000513284.1:p.Cys832Trp
|
|
ENST00000697375.1:n.4728T>G
|
|
|
ENST00000697376.1:c.*16T>G
|
ENSP00000513285.1:n.*16T>G
|
|
ENST00000697377.1:c.2334T>G
|
ENSP00000513286.1:p.Cys778Trp
|
|
ENST00000697378.1:n.3901T>G
|
|
|
ENST00000697379.1:c.2496T>G
|
ENSP00000513287.1:p.Cys832Trp
|
|
ENST00000697380.1:n.2585T>G
|
|
|
ENST00000697381.1:n.2076T>G
|
|
|
ENST00000697382.1:c.*158T>G
|
ENSP00000513288.1:n.*158T>G
|
|
ENST00000697383.1:c.915T>G
|
ENSP00000513289.1:p.Cys305Trp
|
|
ENST00000261584.9:c.3381T>G
MANE Select
|
ENSP00000261584.4:p.Cys1127Trp
|
|
ENST00000261584.8:c.3381T>G
|
ENSP00000261584.4:p.Cys1127Trp
|
|
ENST00000566069.5:c.147T>G
|
|
|
ENST00000568219.5:c.2496T>G
|
ENSP00000454703.2:p.Cys832Trp
|
|
NM_024675.3:c.3381T>G , LRG_308t1:c.3381T>G
|
NP_078951.2:p.Cys1127Trp
|
|
XM_011545946.1:c.3387T>G
|
XP_011544248.1:p.Cys1129Trp
|
|
XM_011545947.1:c.*16T>G
|
XP_011544249.1:n.*16T>G
|
|
XM_011545948.1:c.2496T>G
|
XP_011544250.1:p.Cys832Trp
|
|
XR_950851.1:n.4089T>G
|
|
|
XM_011545946.2:c.3387T>G
|
XP_011544248.1:p.Cys1129Trp
|
|
XM_011545947.2:c.*16T>G
|
XP_011544249.1:n.*16T>G
|
|
XM_011545948.2:c.2496T>G
|
XP_011544250.1:p.Cys832Trp
|
|
XM_017023671.1:c.3150T>G
|
XP_016879160.1:p.Cys1050Trp
|
|
XM_017023672.2:c.3144T>G
|
XP_016879161.1:p.Cys1048Trp
|
|
XM_017023673.2:c.*16T>G
|
XP_016879162.1:n.*16T>G
|
|
NM_024675.4:c.3381T>G
MANE Select
|
NP_078951.2:p.Cys1127Trp
|
|