|
ENST00000647720.2:c.3403T>G
|
ENSP00000497673.2:p.Leu1135Val
|
|
|
ENST00000647978.2:c.*3117T>G
|
ENSP00000497658.1:n.*3117T>G
|
|
|
ENST00000649781.2:c.3220T>G
|
ENSP00000497203.1:p.Leu1074Val
|
|
|
ENST00000685018.2:c.3403T>G
|
ENSP00000510194.2:p.Leu1135Val
|
|
|
ENST00000687278.2:c.3403T>G
|
ENSP00000509593.2:p.Leu1135Val
|
|
|
ENST00000699585.1:c.3403T>G
|
ENSP00000514456.1:p.Leu1135Val
|
|
|
ENST00000699598.1:c.3403T>G
|
ENSP00000514467.1:p.Leu1135Val
|
|
|
ENST00000699599.1:c.3403T>G
|
ENSP00000514468.1:p.Leu1135Val
|
|
|
ENST00000699600.1:c.3403T>G
|
ENSP00000514469.1:p.Leu1135Val
|
|
|
ENST00000699601.1:c.*1778T>G
|
ENSP00000514470.1:n.*1778T>G
|
|
|
ENST00000699602.1:c.3397T>G
|
ENSP00000514471.1:p.Leu1133Val
|
|
|
ENST00000699604.1:c.*3227T>G
|
ENSP00000514472.1:n.*3227T>G
|
|
|
ENST00000699605.1:c.2977T>G
|
ENSP00000514473.1:p.Leu993Val
|
|
|
ENST00000685018.1:c.151T>G
|
ENSP00000510194.1:p.Leu51Val
|
|
|
ENST00000687278.1:c.994T>G
|
ENSP00000509593.1:p.Leu332Val
|
|
|
ENST00000003084.11:c.3403T>G
MANE Select
|
ENSP00000003084.6:p.Leu1135Val
|
|
|
ENST00000647720.1:c.1053T>G
|
|
|
|
ENST00000648260.1:c.2185T>G
|
ENSP00000497957.1:p.Leu729Val
|
|
|
ENST00000649406.1:c.3220T>G
|
ENSP00000497965.1:p.Leu1074Val
|
|
|
ENST00000649781.1:c.3220T>G
|
ENSP00000497203.1:p.Leu1074Val
|
|
|
ENST00000003084.10:c.3403T>G
|
ENSP00000003084.6:p.Leu1135Val
|
|
|
ENST00000426809.5:c.3313T>G
|
ENSP00000389119.1:p.Leu1105Val
|
|
|
ENST00000468795.1:c.228T>G
|
|
|
|
NM_000492.3:c.3403T>G , LRG_663t1:c.3403T>G
|
NP_000483.3:p.Leu1135Val
|
|
|
XM_011515751.1:c.3493T>G
|
XP_011514053.1:p.Leu1165Val
|
|
|
XM_011515752.1:c.3493T>G
|
XP_011514054.1:p.Leu1165Val
|
|
|
XM_011515753.1:c.3160T>G
|
XP_011514055.1:p.Leu1054Val
|
|
|
XM_011515754.1:c.3160T>G
|
XP_011514056.1:p.Leu1054Val
|
|
|
NM_000492.4:c.3403T>G
MANE Select
|
NP_000483.3:p.Leu1135Val
|
|
