ENST00000647720.2:c.3517+29C>G
|
ENSP00000497673.2:n.3517+29C>G
|
|
ENST00000647978.2:c.*3260C>G
|
ENSP00000497658.1:n.*3260C>G
|
|
ENST00000649781.2:c.3363C>G
|
ENSP00000497203.1:p.Tyr1121Ter
|
|
ENST00000685018.2:c.3546C>G
|
ENSP00000510194.2:p.Tyr1182Ter
|
|
ENST00000687278.2:c.*199C>G
|
ENSP00000509593.2:n.*199C>G
|
|
ENST00000699585.1:c.3517+29C>G
|
ENSP00000514456.1:n.3517+29C>G
|
|
ENST00000699598.1:c.3546C>G
|
ENSP00000514467.1:p.Tyr1182Ter
|
|
ENST00000699599.1:c.3546C>G
|
ENSP00000514468.1:p.Tyr1182Ter
|
|
ENST00000699600.1:c.*207C>G
|
ENSP00000514469.1:n.*207C>G
|
|
ENST00000699601.1:c.*1921C>G
|
ENSP00000514470.1:n.*1921C>G
|
|
ENST00000699602.1:c.3540C>G
|
ENSP00000514471.1:p.Tyr1180Ter
|
|
ENST00000699604.1:c.*3370C>G
|
ENSP00000514472.1:n.*3370C>G
|
|
ENST00000699605.1:c.3120C>G
|
ENSP00000514473.1:p.Tyr1040Ter
|
|
ENST00000685018.1:c.294C>G
|
ENSP00000510194.1:p.Tyr98Ter
|
|
ENST00000687278.1:c.1333C>G
|
ENSP00000509593.1:n.1333C>G
|
|
ENST00000689011.1:c.128C>G
|
|
|
ENST00000003084.11:c.3546C>G
MANE Select
|
ENSP00000003084.6:p.Tyr1182Ter
|
|
ENST00000647720.1:c.1167+29C>G
|
|
|
ENST00000648260.1:c.2328C>G
|
ENSP00000497957.1:p.Tyr776Ter
|
|
ENST00000649406.1:c.3363C>G
|
ENSP00000497965.1:p.Tyr1121Ter
|
|
ENST00000649781.1:c.3363C>G
|
ENSP00000497203.1:p.Tyr1121Ter
|
|
ENST00000003084.10:c.3546C>G
|
ENSP00000003084.6:p.Tyr1182Ter
|
|
ENST00000426809.5:c.3456C>G
|
ENSP00000389119.1:p.Tyr1152Ter
|
|
ENST00000468795.1:c.371C>G
|
|
|
NM_000492.3:c.3546C>G , LRG_663t1:c.3546C>G
|
NP_000483.3:p.Tyr1182Ter
|
|
XM_011515751.1:c.3636C>G
|
XP_011514053.1:p.Tyr1212Ter
|
|
XM_011515752.1:c.3636C>G
|
XP_011514054.1:p.Tyr1212Ter
|
|
XM_011515753.1:c.3303C>G
|
XP_011514055.1:p.Tyr1101Ter
|
|
XM_011515754.1:c.3303C>G
|
XP_011514056.1:p.Tyr1101Ter
|
|
NM_000492.4:c.3546C>G
MANE Select
|
NP_000483.3:p.Tyr1182Ter
|
|