ENST00000556394.2:c.541C>G
|
ENSP00000451967.2:p.Pro181Ala
|
|
ENST00000557289.2:c.298C>G
|
|
|
ENST00000682247.1:c.1000C>G
|
ENSP00000507213.1:p.Pro334Ala
|
|
ENST00000682382.1:c.572C>G
|
|
|
ENST00000682395.1:n.729C>G
|
|
|
ENST00000682459.1:n.664C>G
|
|
|
ENST00000682467.1:c.1000C>G
|
ENSP00000508062.1:p.Pro334Ala
|
|
ENST00000682795.1:c.1000C>G
|
ENSP00000507574.1:p.Pro334Ala
|
|
ENST00000682895.1:n.716C>G
|
|
|
ENST00000682955.1:n.288C>G
|
|
|
ENST00000683188.1:c.526C>G
|
|
|
ENST00000683300.1:c.110-2422C>G
|
ENSP00000507630.1:n.110-2422C>G
|
|
ENST00000683328.1:c.109+5997C>G
|
ENSP00000508096.1:n.109+5997C>G
|
|
ENST00000683380.1:n.664C>G
|
|
|
ENST00000683551.1:c.186C>G
|
|
|
ENST00000683828.1:c.709C>G
|
|
|
ENST00000684259.1:n.851C>G
|
|
|
ENST00000684549.1:n.551C>G
|
|
|
ENST00000684554.1:c.237C>G
|
|
|
ENST00000261534.9:c.1000C>G
MANE Select
|
ENSP00000261534.4:p.Pro334Ala
|
|
ENST00000261534.8:c.1000C>G
|
ENSP00000261534.4:p.Pro334Ala
|
|
ENST00000452340.7:n.1023C>G
|
|
|
ENST00000554767.5:n.1786C>G
|
|
|
ENST00000557289.1:c.239C>G
|
ENSP00000451115.1:n.239C>G
|
|
NM_013382.5:c.1000C>G , LRG_844t1:c.1000C>G
|
NP_037514.2:p.Pro334Ala
|
|
XM_011536675.1:c.1000C>G
|
XP_011534977.1:p.Pro334Ala
|
|
XM_011536676.1:c.667C>G
|
XP_011534978.1:p.Pro223Ala
|
|
XM_011536677.1:c.548-2422C>G
|
XP_011534979.1:n.548-2422C>G
|
|
XM_011536678.1:c.1000C>G
|
XP_011534980.1:p.Pro334Ala
|
|
XM_011536679.1:c.94C>G
|
XP_011534981.1:p.Pro32Ala
|
|
XM_011536680.1:c.1000C>G
|
XP_011534982.1:p.Pro334Ala
|
|
XR_943416.1:n.1203C>G
|
|
|
XM_011536675.2:c.1000C>G
|
XP_011534977.1:p.Pro334Ala
|
|
XM_011536676.2:c.667C>G
|
XP_011534978.1:p.Pro223Ala
|
|
XM_011536677.3:c.548-2422C>G
|
XP_011534979.1:n.548-2422C>G
|
|
XR_001750279.1:n.1200C>G
|
|
|
XR_001750282.1:n.1204C>G
|
|
|
XR_943416.3:n.1201C>G
|
|
|
NM_013382.6:c.1000C>G
|
NP_037514.2:p.Pro334Ala
|
|
NM_013382.7:c.1000C>G
MANE Select
|
NP_037514.2:p.Pro334Ala
|
|