|
ENST00000271643.9:c.1996G>T
(ADAMTSL4)
MANE Select
|
ENSP00000271643.4:p.Ala666Ser
|
|
|
ENST00000674043.1:c.2065G>T
(ADAMTSL4)
|
ENSP00000501295.1:p.Ala689Ser
|
|
|
ENST00000674058.1:c.1879G>T
(ADAMTSL4)
|
ENSP00000501255.1:p.Ala627Ser
|
|
|
ENST00000271643.8:c.1996G>T
(ADAMTSL4)
|
ENSP00000271643.4:p.Ala666Ser
|
|
|
ENST00000369038.6:c.1996G>T
(ADAMTSL4)
|
ENSP00000358034.2:p.Ala666Ser
|
|
|
ENST00000369039.9:c.2065G>T
(ADAMTSL4)
|
ENSP00000358035.5:p.Ala689Ser
|
|
|
ENST00000369041.9:c.1996G>T
(ADAMTSL4)
|
ENSP00000358037.5:p.Ala666Ser
|
|
|
ENST00000622417.4:c.610G>T
(ADAMTSL4)
|
ENSP00000477897.1:p.Ala204Ser
|
|
|
NM_001288607.1:c.1879G>T
(ADAMTSL4)
|
NP_001275536.1:p.Ala627Ser
|
|
|
NM_001288608.1:c.2065G>T
(ADAMTSL4)
|
NP_001275537.1:p.Ala689Ser
|
|
|
NM_019032.5:c.1996G>T
(ADAMTSL4)
|
NP_061905.2:p.Ala666Ser
|
|
|
NM_025008.4:c.1996G>T
(ADAMTSL4)
|
NP_079284.2:p.Ala666Ser
|
|
|
XM_011509644.1:c.2164G>T
(ADAMTSL4)
|
XP_011507946.1:p.Ala722Ser
|
|
|
XM_011509645.1:c.2095G>T
(ADAMTSL4)
|
XP_011507947.1:p.Ala699Ser
|
|
|
XM_011509646.1:c.2065G>T
(ADAMTSL4)
|
XP_011507948.1:p.Ala689Ser
|
|
|
XM_011509647.1:c.2065G>T
(ADAMTSL4)
|
XP_011507949.1:p.Ala689Ser
|
|
|
XM_011509648.1:c.2065G>T
(ADAMTSL4)
|
XP_011507950.1:p.Ala689Ser
|
|
|
XM_011509649.1:c.2164G>T
(ADAMTSL4)
|
XP_011507951.1:p.Ala722Ser
|
|
|
XM_011509650.1:c.2164G>T
(ADAMTSL4)
|
XP_011507952.1:p.Ala722Ser
|
|
|
XM_011509651.1:c.673G>T
(ADAMTSL4)
|
XP_011507953.1:p.Ala225Ser
|
|
|
XM_011509652.1:c.673G>T
(ADAMTSL4)
|
XP_011507954.1:p.Ala225Ser
|
|
|
XR_921844.1:n.2349G>T
(ADAMTSL4)
|
|
|
|
XR_922133.1:n.139+409C>A
(ADAMTSL4-AS2)
|
|
|
|
XM_011509644.3:c.2164G>T
(ADAMTSL4)
|
XP_011507946.1:p.Ala722Ser
|
|
|
XM_011509645.3:c.2095G>T
(ADAMTSL4)
|
XP_011507947.1:p.Ala699Ser
|
|
|
XM_011509648.3:c.2065G>T
(ADAMTSL4)
|
XP_011507950.1:p.Ala689Ser
|
|
|
XM_011509649.3:c.2164G>T
(ADAMTSL4)
|
XP_011507951.1:p.Ala722Ser
|
|
|
XM_011509650.3:c.2164G>T
(ADAMTSL4)
|
XP_011507952.1:p.Ala722Ser
|
|
|
XM_011509651.2:c.673G>T
(ADAMTSL4)
|
XP_011507953.1:p.Ala225Ser
|
|
|
XM_011509652.2:c.673G>T
(ADAMTSL4)
|
XP_011507954.1:p.Ala225Ser
|
|
|
XM_017001506.2:c.2065G>T
(ADAMTSL4)
|
XP_016856995.1:p.Ala689Ser
|
|
|
XM_017001507.1:c.409G>T
(ADAMTSL4)
|
XP_016856996.1:p.Ala137Ser
|
|
|
XR_001737242.2:n.2149G>T
(ADAMTSL4)
|
|
|
|
XR_921844.3:n.2322G>T
(ADAMTSL4)
|
|
|
|
NM_001288607.2:c.1879G>T
(ADAMTSL4)
|
NP_001275536.1:p.Ala627Ser
|
|
|
NM_025008.5:c.1996G>T
(ADAMTSL4)
|
NP_079284.2:p.Ala666Ser
|
|
|
NM_001288608.2:c.2065G>T
(ADAMTSL4)
|
NP_001275537.1:p.Ala689Ser
|
|
|
NM_001378596.1:c.1996G>T
(ADAMTSL4)
|
NP_001365525.1:p.Ala666Ser
|
|
|
NM_019032.6:c.1996G>T
(ADAMTSL4)
MANE Select
|
NP_061905.2:p.Ala666Ser
|
|
