|
ENST00000361166.10:c.675+2841C>G
|
ENSP00000354529.6:n.675+2841C>G
|
|
|
ENST00000673312.2:c.*170-100C>G
|
ENSP00000500186.2:n.*170-100C>G
|
|
|
ENST00000338641.10:c.676-100C>G
MANE Select
|
ENSP00000344666.5:n.676-100C>G
|
|
|
ENST00000361166.9:c.228+2841C>G
|
ENSP00000354529.5:n.228+2841C>G
|
|
|
ENST00000672461.1:c.676-100C>G
|
ENSP00000500919.1:n.676-100C>G
|
|
|
ENST00000672805.1:c.*558-100C>G
|
ENSP00000500295.1:n.*558-100C>G
|
|
|
ENST00000672896.1:c.676-100C>G
|
ENSP00000500117.1:n.676-100C>G
|
|
|
ENST00000673312.1:c.695-100C>G
|
ENSP00000500186.1:n.695-100C>G
|
|
|
ENST00000334961.11:c.427-100C>G
|
ENSP00000335652.7:n.427-100C>G
|
|
|
ENST00000338641.8:c.676-100C>G
|
ENSP00000344666.4:n.676-100C>G
|
|
|
ENST00000353887.8:c.427-100C>G
|
ENSP00000340626.4:n.427-100C>G
|
|
|
ENST00000361166.8:c.676-100C>G
|
ENSP00000354529.4:n.676-100C>G
|
|
|
ENST00000361452.8:c.553-100C>G
|
ENSP00000354897.4:n.553-100C>G
|
|
|
ENST00000361676.8:c.550-100C>G
|
ENSP00000355183.4:n.550-100C>G
|
|
|
ENST00000397789.3:c.676-100C>G
|
ENSP00000380891.3:n.676-100C>G
|
|
|
ENST00000403435.5:c.676-100C>G
|
ENSP00000384029.1:n.676-100C>G
|
|
|
ENST00000403999.7:c.676-100C>G
|
ENSP00000384797.3:n.676-100C>G
|
|
|
ENST00000413209.6:c.447+18820C>G
|
ENSP00000409921.2:n.447+18820C>G
|
|
|
ENST00000432151.5:c.199-100C>G
|
ENSP00000395885.1:n.199-100C>G
|
|
|
NM_000268.3:c.676-100C>G , LRG_511t1:c.676-100C>G
|
NP_000259.1:n.676-100C>G
|
|
|
NM_016418.5:c.676-100C>G , LRG_511t2:c.676-100C>G
|
NP_057502.2:n.676-100C>G
|
|
|
NM_181825.2:c.676-100C>G
|
NP_861546.1:n.676-100C>G
|
|
|
NM_181828.2:c.550-100C>G
|
NP_861966.1:n.550-100C>G
|
|
|
NM_181829.2:c.553-100C>G
|
NP_861967.1:n.553-100C>G
|
|
|
NM_181830.2:c.427-100C>G
|
NP_861968.1:n.427-100C>G
|
|
|
NM_181831.2:c.427-100C>G
|
NP_861969.1:n.427-100C>G
|
|
|
NM_181832.2:c.676-100C>G
|
NP_861970.1:n.676-100C>G
|
|
|
NM_181833.2:c.447+18820C>G
|
NP_861971.1:n.447+18820C>G
|
|
|
NR_156186.1:n.1235-100C>G
|
|
|
|
XM_017028809.2:c.562-100C>G
|
XP_016884298.1:n.562-100C>G
|
|
|
XM_017028810.1:c.562-100C>G
|
XP_016884299.1:n.562-100C>G
|
|
|
NM_000268.4:c.676-100C>G
MANE Select
|
NP_000259.1:n.676-100C>G
|
|
|
NM_181825.3:c.676-100C>G
|
NP_861546.1:n.676-100C>G
|
|
|
NM_181828.3:c.550-100C>G
|
NP_861966.1:n.550-100C>G
|
|
|
NM_181829.3:c.553-100C>G
|
NP_861967.1:n.553-100C>G
|
|
|
NM_181830.3:c.427-100C>G
|
NP_861968.1:n.427-100C>G
|
|
|
NM_181831.3:c.427-100C>G
|
NP_861969.1:n.427-100C>G
|
|
|
NM_181832.3:c.676-100C>G
|
NP_861970.1:n.676-100C>G
|
|
|
NR_156186.2:n.1158-100C>G
|
|
|
|
NM_181833.3:c.447+18820C>G
|
NP_861971.1:n.447+18820C>G
|
|
