|
ENST00000507260.3:n.343T>A
|
|
|
|
ENST00000626637.2:c.269T>A
|
ENSP00000486771.1:p.Leu90His
|
|
|
ENST00000638648.2:c.269T>A
|
ENSP00000507949.1:p.Leu90His
|
|
|
ENST00000640201.2:n.343T>A
|
|
|
|
ENST00000640752.2:n.343T>A
|
|
|
|
ENST00000681992.1:n.294T>A
|
|
|
|
ENST00000682067.1:c.217T>A
|
|
|
|
ENST00000682197.1:n.341T>A
|
|
|
|
ENST00000682373.1:c.201T>A
|
|
|
|
ENST00000684696.1:c.257T>A
|
ENSP00000507675.1:p.Leu86His
|
|
|
ENST00000309522.8:c.257T>A
MANE Select
|
ENSP00000312288.4:p.Leu86His
|
|
|
ENST00000403312.6:c.257T>A
|
ENSP00000385638.3:p.Leu86His
|
|
|
ENST00000505878.4:c.434T>A
|
ENSP00000425952.2:p.Leu145His
|
|
|
ENST00000507260.2:n.300T>A
|
|
|
|
ENST00000638559.1:c.120-4548T>A
|
|
|
|
ENST00000638621.1:c.133-13591T>A
|
ENSP00000491581.1:n.133-13591T>A
|
|
|
ENST00000638648.1:n.408T>A
|
|
|
|
ENST00000639146.1:c.257T>A
|
ENSP00000492345.1:p.Leu86His
|
|
|
ENST00000639335.1:c.257T>A
|
ENSP00000491310.1:p.Leu86His
|
|
|
ENST00000639698.1:c.137T>A
|
ENSP00000492420.1:p.Leu46His
|
|
|
ENST00000639784.1:c.121T>A
|
|
|
|
ENST00000640048.1:c.95T>A
|
ENSP00000492009.1:p.Leu32His
|
|
|
ENST00000640060.1:c.*352T>A
|
ENSP00000492734.1:n.*352T>A
|
|
|
ENST00000640201.1:n.212T>A
|
|
|
|
ENST00000640586.1:c.546T>A
|
|
|
|
ENST00000640752.1:n.336T>A
|
|
|
|
ENST00000309522.7:c.257T>A
|
ENSP00000312288.3:p.Leu86His
|
|
|
ENST00000403312.5:c.434T>A
|
ENSP00000385638.2:p.Leu145His
|
|
|
ENST00000505878.3:c.269T>A
|
ENSP00000425952.1:p.Leu90His
|
|
|
ENST00000603302.5:c.257T>A
|
ENSP00000474560.1:p.Leu86His
|
|
|
ENST00000626637.1:c.269T>A
|
ENSP00000486771.1:p.Leu90His
|
|
|
XM_005262972.1:c.269T>A
|
XP_005263029.1:p.Leu90His
|
|
|
XR_938726.1:n.406T>A
|
|
|
|
XR_001741214.2:n.351T>A
|
|
|
|
XR_002959727.1:n.351T>A
|
|
|
|
NM_005327.7:c.257T>A
MANE Select
|
NP_005318.6:p.Leu86His
|
|
|
NM_001184705.4:c.257T>A
|
NP_001171634.3:p.Leu86His
|
|
|
NM_001331027.2:c.269T>A
|
NP_001317956.2:p.Leu90His
|
|
