ENST00000553863.6:c.121C=
|
ENSP00000508202.1:p.Pro41=
|
|
ENST00000556394.2:c.358-1677C=
|
ENSP00000451967.2:n.358-1677C=
|
|
ENST00000556880.6:n.692C=
|
|
|
ENST00000557289.2:c.12C=
|
|
|
ENST00000682247.1:c.668C=
|
ENSP00000507213.1:p.Ala223=
|
|
ENST00000682382.1:c.496-2467C=
|
|
|
ENST00000682395.1:n.397C=
|
|
|
ENST00000682459.1:n.332C=
|
|
|
ENST00000682467.1:c.668C=
|
ENSP00000508062.1:p.Ala223=
|
|
ENST00000682795.1:c.668C=
|
ENSP00000507574.1:p.Ala223=
|
|
ENST00000682895.1:n.384C=
|
|
|
ENST00000682955.1:n.212-2467C=
|
|
|
ENST00000683167.1:c.12C=
|
|
|
ENST00000683188.1:c.343-1677C=
|
|
|
ENST00000683300.1:c.109+3454C=
|
ENSP00000507630.1:n.109+3454C=
|
|
ENST00000683328.1:c.109+3454C=
|
ENSP00000508096.1:n.109+3454C=
|
|
ENST00000683380.1:n.332C=
|
|
|
ENST00000683398.1:c.12C=
|
|
|
ENST00000683551.1:c.109+1597C=
|
|
|
ENST00000683828.1:c.525+1597C=
|
|
|
ENST00000684259.1:n.519C=
|
|
|
ENST00000684549.1:n.368-1677C=
|
|
|
ENST00000684554.1:c.12C=
|
|
|
ENST00000261534.9:c.668C=
MANE Select
|
ENSP00000261534.4:p.Ala223=
|
|
ENST00000261534.8:c.668C=
|
ENSP00000261534.4:p.Ala223=
|
|
ENST00000452340.7:n.691C=
|
|
|
ENST00000553863.5:n.332C=
|
|
|
ENST00000554948.1:c.395C=
|
ENSP00000452060.1:p.Ala132=
|
|
ENST00000555675.5:n.384C=
|
|
|
ENST00000556326.5:c.*334C=
|
ENSP00000450630.1:n.*334C=
|
|
ENST00000557289.1:c.56-1677C=
|
ENSP00000451115.1:n.56-1677C=
|
|
NM_013382.5:c.668C= , LRG_844t1:c.668C=
|
NP_037514.2:p.Ala223=
|
|
XM_011536675.1:c.668C=
|
XP_011534977.1:p.Ala223=
|
|
XM_011536676.1:c.335C=
|
XP_011534978.1:p.Ala112=
|
|
XM_011536677.1:c.547+3454C=
|
XP_011534979.1:n.547+3454C=
|
|
XM_011536678.1:c.668C=
|
XP_011534980.1:p.Ala223=
|
|
XM_011536679.1:c.-90-1677C=
|
XP_011534981.1:n.-90-1677C=
|
|
XM_011536680.1:c.668C=
|
XP_011534982.1:p.Ala223=
|
|
XR_943416.1:n.871C=
|
|
|
XM_011536675.2:c.668C=
|
XP_011534977.1:p.Ala223=
|
|
XM_011536676.2:c.335C=
|
XP_011534978.1:p.Ala112=
|
|
XM_011536677.3:c.547+3454C=
|
XP_011534979.1:n.547+3454C=
|
|
XR_001750279.1:n.868C=
|
|
|
XR_001750282.1:n.872C=
|
|
|
XR_943416.3:n.869C=
|
|
|
NM_013382.6:c.668C=
|
NP_037514.2:p.Ala223=
|
|
NM_013382.7:c.668C=
MANE Select
|
NP_037514.2:p.Ala223=
|
|