|
ENST00000561514.3:c.2918G>T
|
ENSP00000460666.3:p.Gly973Val
|
|
|
ENST00000565038.2:c.*393G>T
|
ENSP00000459882.2:n.*393G>T
|
|
|
ENST00000566069.6:c.2912G>T
|
ENSP00000459237.2:p.Gly971Val
|
|
|
ENST00000697377.2:c.2756G>T
|
ENSP00000513286.2:p.Gly919Val
|
|
|
ENST00000697379.2:c.2918G>T
|
ENSP00000513287.2:p.Gly973Val
|
|
|
ENST00000561514.2:c.2027G>T
|
ENSP00000460666.2:p.Gly676Val
|
|
|
ENST00000697374.1:c.2027G>T
|
ENSP00000513284.1:p.Gly676Val
|
|
|
ENST00000697375.1:n.4259G>T
|
|
|
|
ENST00000697376.1:c.2027G>T
|
ENSP00000513285.1:p.Gly676Val
|
|
|
ENST00000697377.1:c.1865G>T
|
ENSP00000513286.1:p.Gly622Val
|
|
|
ENST00000697378.1:n.3432G>T
|
|
|
|
ENST00000697379.1:c.2027G>T
|
ENSP00000513287.1:p.Gly676Val
|
|
|
ENST00000697380.1:n.2204G>T
|
|
|
|
ENST00000697381.1:n.1607G>T
|
|
|
|
ENST00000697382.1:c.2027G>T
|
ENSP00000513288.1:p.Gly676Val
|
|
|
ENST00000697383.1:c.446G>T
|
ENSP00000513289.1:p.Gly149Val
|
|
|
ENST00000261584.9:c.2912G>T
MANE Select
|
ENSP00000261584.4:p.Gly971Val
|
|
|
ENST00000261584.8:c.2912G>T
|
ENSP00000261584.4:p.Gly971Val
|
|
|
ENST00000568219.5:c.2027G>T
|
ENSP00000454703.2:p.Gly676Val
|
|
|
NM_024675.3:c.2912G>T , LRG_308t1:c.2912G>T
|
NP_078951.2:p.Gly971Val
|
|
|
XM_011545946.1:c.2918G>T
|
XP_011544248.1:p.Gly973Val
|
|
|
XM_011545947.1:c.2918G>T
|
XP_011544249.1:p.Gly973Val
|
|
|
XM_011545948.1:c.2027G>T
|
XP_011544250.1:p.Gly676Val
|
|
|
XR_950851.1:n.3708G>T
|
|
|
|
XM_011545946.2:c.2918G>T
|
XP_011544248.1:p.Gly973Val
|
|
|
XM_011545947.2:c.2918G>T
|
XP_011544249.1:p.Gly973Val
|
|
|
XM_011545948.2:c.2027G>T
|
XP_011544250.1:p.Gly676Val
|
|
|
XM_017023671.1:c.2918G>T
|
XP_016879160.1:p.Gly973Val
|
|
|
XM_017023672.2:c.2912G>T
|
XP_016879161.1:p.Gly971Val
|
|
|
XM_017023673.2:c.2912G>T
|
XP_016879162.1:p.Gly971Val
|
|
|
NM_024675.4:c.2912G>T
MANE Select
|
NP_078951.2:p.Gly971Val
|
|
