ENST00000328381.10:c.770G>C
MANE Select
|
ENSP00000328340.5:p.Trp257Ser
|
|
ENST00000324689.8:c.607G>C
|
ENSP00000323693.4:p.Gly203Arg
|
|
ENST00000328381.9:c.770G>C
|
ENSP00000328340.5:p.Trp257Ser
|
|
ENST00000443677.6:c.463G>C
|
ENSP00000411965.2:p.Gly155Arg
|
|
ENST00000535306.6:c.835G>C
|
ENSP00000440470.2:p.Gly279Arg
|
|
NM_001184992.1:c.835G>C
|
NP_001171921.1:p.Gly279Arg
|
|
NM_032322.3:c.770G>C
|
NP_115698.3:p.Trp257Ser
|
|
NM_197939.1:c.607G>C
|
NP_922921.1:p.Gly203Arg
|
|
XM_005258043.3:c.227G>C
|
XP_005258100.1:p.Trp76Ser
|
|
XM_006722138.2:c.449G>C
|
XP_006722201.1:p.Trp150Ser
|
|
XM_017025223.1:c.227G>C
|
XP_016880712.1:p.Trp76Ser
|
|
XM_024451000.1:c.227G>C
|
XP_024306768.1:p.Trp76Ser
|
|
XM_024451001.1:c.227G>C
|
XP_024306769.1:p.Trp76Ser
|
|
XR_002958076.1:n.1103G>C
|
|
|
XR_002958077.1:n.1038G>C
|
|
|
XR_002958078.1:n.875G>C
|
|
|
NM_032322.4:c.770G>C
MANE Select
|
NP_115698.3:p.Trp257Ser
|
|
NM_001184992.2:c.835G>C
|
NP_001171921.1:p.Gly279Arg
|
|
NM_197939.2:c.607G>C
|
NP_922921.1:p.Gly203Arg
|
|