ENST00000361166.10:c.798G>C
|
ENSP00000354529.6:p.Arg266Ser
|
|
ENST00000673312.2:c.*427G>C
|
ENSP00000500186.2:n.*427G>C
|
|
ENST00000338641.10:c.933G>C
MANE Select
|
ENSP00000344666.5:p.Arg311Ser
|
|
ENST00000361166.9:c.351G>C
|
ENSP00000354529.5:p.Arg117Ser
|
|
ENST00000672461.1:c.933G>C
|
ENSP00000500919.1:p.Arg311Ser
|
|
ENST00000672805.1:c.*815G>C
|
ENSP00000500295.1:n.*815G>C
|
|
ENST00000672896.1:c.933G>C
|
ENSP00000500117.1:p.Arg311Ser
|
|
ENST00000673312.1:c.952G>C
|
ENSP00000500186.1:n.952G>C
|
|
ENST00000334961.11:c.684G>C
|
ENSP00000335652.7:p.Arg228Ser
|
|
ENST00000338641.8:c.933G>C
|
ENSP00000344666.4:p.Arg311Ser
|
|
ENST00000353887.8:c.684G>C
|
ENSP00000340626.4:p.Arg228Ser
|
|
ENST00000361166.8:c.933G>C
|
ENSP00000354529.4:p.Arg311Ser
|
|
ENST00000361452.8:c.810G>C
|
ENSP00000354897.4:p.Arg270Ser
|
|
ENST00000361676.8:c.807G>C
|
ENSP00000355183.4:p.Arg269Ser
|
|
ENST00000397789.3:c.933G>C
|
ENSP00000380891.3:p.Arg311Ser
|
|
ENST00000403435.5:c.933G>C
|
ENSP00000384029.1:p.Arg311Ser
|
|
ENST00000403999.7:c.933G>C
|
ENSP00000384797.3:p.Arg311Ser
|
|
ENST00000413209.6:c.447+26095G>C
|
ENSP00000409921.2:n.447+26095G>C
|
|
ENST00000432151.5:c.456G>C
|
ENSP00000395885.1:p.Arg152Ser
|
|
NM_000268.3:c.933G>C , LRG_511t1:c.933G>C
|
NP_000259.1:p.Arg311Ser
|
|
NM_016418.5:c.933G>C , LRG_511t2:c.933G>C
|
NP_057502.2:p.Arg311Ser
|
|
NM_181825.2:c.933G>C
|
NP_861546.1:p.Arg311Ser
|
|
NM_181828.2:c.807G>C
|
NP_861966.1:p.Arg269Ser
|
|
NM_181829.2:c.810G>C
|
NP_861967.1:p.Arg270Ser
|
|
NM_181830.2:c.684G>C
|
NP_861968.1:p.Arg228Ser
|
|
NM_181831.2:c.684G>C
|
NP_861969.1:p.Arg228Ser
|
|
NM_181832.2:c.933G>C
|
NP_861970.1:p.Arg311Ser
|
|
NM_181833.2:c.447+26095G>C
|
NP_861971.1:n.447+26095G>C
|
|
NR_156186.1:n.1492G>C
|
|
|
XM_017028809.2:c.819G>C
|
XP_016884298.1:p.Arg273Ser
|
|
XM_017028810.1:c.819G>C
|
XP_016884299.1:p.Arg273Ser
|
|
NM_000268.4:c.933G>C
MANE Select
|
NP_000259.1:p.Arg311Ser
|
|
NM_181825.3:c.933G>C
|
NP_861546.1:p.Arg311Ser
|
|
NM_181828.3:c.807G>C
|
NP_861966.1:p.Arg269Ser
|
|
NM_181829.3:c.810G>C
|
NP_861967.1:p.Arg270Ser
|
|
NM_181830.3:c.684G>C
|
NP_861968.1:p.Arg228Ser
|
|
NM_181831.3:c.684G>C
|
NP_861969.1:p.Arg228Ser
|
|
NM_181832.3:c.933G>C
|
NP_861970.1:p.Arg311Ser
|
|
NR_156186.2:n.1415G>C
|
|
|
NM_181833.3:c.447+26095G>C
|
NP_861971.1:n.447+26095G>C
|
|