ENST00000647720.2:c.3491T>G
|
ENSP00000497673.2:p.Phe1164Cys
|
|
ENST00000647978.2:c.*3205T>G
|
ENSP00000497658.1:n.*3205T>G
|
|
ENST00000649781.2:c.3308T>G
|
ENSP00000497203.1:p.Phe1103Cys
|
|
ENST00000685018.2:c.3491T>G
|
ENSP00000510194.2:p.Phe1164Cys
|
|
ENST00000687278.2:c.*144T>G
|
ENSP00000509593.2:n.*144T>G
|
|
ENST00000699585.1:c.3491T>G
|
ENSP00000514456.1:p.Phe1164Cys
|
|
ENST00000699598.1:c.3491T>G
|
ENSP00000514467.1:p.Phe1164Cys
|
|
ENST00000699599.1:c.3491T>G
|
ENSP00000514468.1:p.Phe1164Cys
|
|
ENST00000699600.1:c.*152T>G
|
ENSP00000514469.1:n.*152T>G
|
|
ENST00000699601.1:c.*1866T>G
|
ENSP00000514470.1:n.*1866T>G
|
|
ENST00000699602.1:c.3485T>G
|
ENSP00000514471.1:p.Phe1162Cys
|
|
ENST00000699604.1:c.*3315T>G
|
ENSP00000514472.1:n.*3315T>G
|
|
ENST00000699605.1:c.3065T>G
|
ENSP00000514473.1:p.Phe1022Cys
|
|
ENST00000685018.1:c.239T>G
|
ENSP00000510194.1:p.Phe80Cys
|
|
ENST00000687278.1:c.1278T>G
|
ENSP00000509593.1:n.1278T>G
|
|
ENST00000689011.1:c.73T>G
|
|
|
ENST00000003084.11:c.3491T>G
MANE Select
|
ENSP00000003084.6:p.Phe1164Cys
|
|
ENST00000647720.1:c.1141T>G
|
|
|
ENST00000648260.1:c.2273T>G
|
ENSP00000497957.1:p.Phe758Cys
|
|
ENST00000649406.1:c.3308T>G
|
ENSP00000497965.1:p.Phe1103Cys
|
|
ENST00000649781.1:c.3308T>G
|
ENSP00000497203.1:p.Phe1103Cys
|
|
ENST00000003084.10:c.3491T>G
|
ENSP00000003084.6:p.Phe1164Cys
|
|
ENST00000426809.5:c.3401T>G
|
ENSP00000389119.1:p.Phe1134Cys
|
|
ENST00000468795.1:c.316T>G
|
|
|
NM_000492.3:c.3491T>G , LRG_663t1:c.3491T>G
|
NP_000483.3:p.Phe1164Cys
|
|
XM_011515751.1:c.3581T>G
|
XP_011514053.1:p.Phe1194Cys
|
|
XM_011515752.1:c.3581T>G
|
XP_011514054.1:p.Phe1194Cys
|
|
XM_011515753.1:c.3248T>G
|
XP_011514055.1:p.Phe1083Cys
|
|
XM_011515754.1:c.3248T>G
|
XP_011514056.1:p.Phe1083Cys
|
|
NM_000492.4:c.3491T>G
MANE Select
|
NP_000483.3:p.Phe1164Cys
|
|