ENST00000647720.2:c.579+128T=
|
ENSP00000497673.2:n.579+128T=
|
|
ENST00000647978.2:c.*476+128T=
|
ENSP00000497658.1:n.*476+128T=
|
|
ENST00000649781.2:c.579+128T=
|
ENSP00000497203.1:n.579+128T=
|
|
ENST00000685018.2:c.579+128T=
|
ENSP00000510194.2:n.579+128T=
|
|
ENST00000687278.2:c.579+128T=
|
ENSP00000509593.2:n.579+128T=
|
|
ENST00000699585.1:c.579+128T=
|
ENSP00000514456.1:n.579+128T=
|
|
ENST00000699596.1:c.579+128T=
|
ENSP00000514465.1:n.579+128T=
|
|
ENST00000699597.1:c.579+128T=
|
ENSP00000514466.1:n.579+128T=
|
|
ENST00000699598.1:c.579+128T=
|
ENSP00000514467.1:n.579+128T=
|
|
ENST00000699599.1:c.579+128T=
|
ENSP00000514468.1:n.579+128T=
|
|
ENST00000699600.1:c.579+128T=
|
ENSP00000514469.1:n.579+128T=
|
|
ENST00000699601.1:c.579+128T=
|
ENSP00000514470.1:n.579+128T=
|
|
ENST00000699602.1:c.579+128T=
|
ENSP00000514471.1:n.579+128T=
|
|
ENST00000699604.1:c.*403+128T=
|
ENSP00000514472.1:n.*403+128T=
|
|
ENST00000699605.1:c.336+128T=
|
ENSP00000514473.1:n.336+128T=
|
|
ENST00000003084.11:c.579+128T=
MANE Select
|
ENSP00000003084.6:n.579+128T=
|
|
ENST00000647978.1:c.*476+128T=
|
ENSP00000497658.1:n.*476+128T=
|
|
ENST00000648260.1:c.579+128T=
|
ENSP00000497957.1:n.579+128T=
|
|
ENST00000649406.1:c.579+128T=
|
ENSP00000497965.1:n.579+128T=
|
|
ENST00000649781.1:c.579+128T=
|
ENSP00000497203.1:n.579+128T=
|
|
ENST00000673785.1:c.336+128T=
|
ENSP00000501235.1:n.336+128T=
|
|
ENST00000003084.10:c.579+128T=
|
ENSP00000003084.6:n.579+128T=
|
|
ENST00000426809.5:c.490-755T=
|
ENSP00000389119.1:n.490-755T=
|
|
NM_000492.3:c.579+128T= , LRG_663t1:c.579+128T=
|
NP_000483.3:n.579+128T=
|
|
XM_011515751.1:c.669+128T=
|
XP_011514053.1:n.669+128T=
|
|
XM_011515752.1:c.669+128T=
|
XP_011514054.1:n.669+128T=
|
|
XM_011515753.1:c.336+128T=
|
XP_011514055.1:n.336+128T=
|
|
XM_011515754.1:c.336+128T=
|
XP_011514056.1:n.336+128T=
|
|
NM_000492.4:c.579+128T=
MANE Select
|
NP_000483.3:n.579+128T=
|
|