|
ENST00000396138.9:c.307G>T
MANE Select
|
ENSP00000379442.5:p.Gly103Cys
|
|
|
ENST00000577168.2:c.307G>T
|
ENSP00000459738.2:p.Gly103Cys
|
|
|
ENST00000302509.8:c.307G>T
|
ENSP00000306279.4:p.Gly103Cys
|
|
|
ENST00000396134.6:c.406G>T
|
ENSP00000379438.2:p.Gly136Cys
|
|
|
ENST00000396138.8:c.454G>T
|
ENSP00000379442.4:p.Gly152Cys
|
|
|
ENST00000570689.5:c.307G>T
|
ENSP00000460548.1:p.Gly103Cys
|
|
|
ENST00000571174.5:c.307G>T
|
ENSP00000458939.1:p.Gly103Cys
|
|
|
ENST00000573567.5:c.376G>T
|
ENSP00000460374.1:p.Gly126Cys
|
|
|
ENST00000574195.5:c.469G>T
|
ENSP00000460845.1:p.Gly157Cys
|
|
|
ENST00000576688.2:c.307G>T
|
|
|
|
ENST00000577168.1:c.391G>T
|
ENSP00000459738.1:p.Gly131Cys
|
|
|
NM_001008389.2:c.307G>T
|
NP_001008390.1:p.Gly103Cys
|
|
|
NM_001278614.1:c.406G>T
|
NP_001265543.1:p.Gly136Cys
|
|
|
NM_003361.3:c.307G>T
|
NP_003352.2:p.Gly103Cys
|
|
|
XM_011545934.1:c.391G>T
|
XP_011544236.1:p.Gly131Cys
|
|
|
XM_011545935.1:c.307G>T
|
XP_011544237.1:p.Gly103Cys
|
|
|
XM_011545936.1:c.307G>T
|
XP_011544238.1:p.Gly103Cys
|
|
|
XM_011545937.1:c.307G>T
|
XP_011544239.1:p.Gly103Cys
|
|
|
XM_011545938.1:c.307G>T
|
XP_011544240.1:p.Gly103Cys
|
|
|
XM_011545939.1:c.391G>T
|
XP_011544241.1:p.Gly131Cys
|
|
|
XM_011545940.1:c.454G>T
|
XP_011544242.1:p.Gly152Cys
|
|
|
XM_011545934.2:c.307G>T
|
XP_011544236.2:p.Gly103Cys
|
|
|
XM_011545940.2:c.307G>T
|
XP_011544242.2:p.Gly103Cys
|
|
|
XM_024450433.1:c.307G>T
|
XP_024306201.1:p.Gly103Cys
|
|
|
NM_001008389.3:c.307G>T
|
NP_001008390.1:p.Gly103Cys
|
|
|
NM_001278614.2:c.406G>T
|
NP_001265543.1:p.Gly136Cys
|
|
|
NM_001378232.1:c.307G>T
|
NP_001365161.1:p.Gly103Cys
|
|
|
NM_001378233.1:c.307G>T
|
NP_001365162.1:p.Gly103Cys
|
|
|
NM_001378234.1:c.307G>T
|
NP_001365163.1:p.Gly103Cys
|
|
|
NM_001378235.1:c.307G>T
|
NP_001365164.1:p.Gly103Cys
|
|
|
NM_001378237.1:c.307G>T
|
NP_001365166.1:p.Gly103Cys
|
|
|
NM_003361.4:c.307G>T
MANE Select
|
NP_003352.2:p.Gly103Cys
|
|
|
NR_165456.1:n.532G>T
|
|
|
