ENST00000356839.10:c.1821T>A
MANE Select
|
ENSP00000349297.5:p.Cys607Ter
|
|
ENST00000322910.9:c.*1776T>A
|
ENSP00000325395.5:n.*1776T>A
|
|
ENST00000350303.9:c.1755T>A
|
ENSP00000344152.5:p.Cys585Ter
|
|
ENST00000356839.9:c.1821T>A
|
ENSP00000349297.5:p.Cys607Ter
|
|
ENST00000542255.6:c.700T>A
|
|
|
ENST00000543245.6:c.1890T>A
|
ENSP00000438689.2:p.Cys630Ter
|
|
ENST00000578033.1:n.246T>A
|
|
|
ENST00000578319.5:n.402T>A
|
|
|
ENST00000578711.1:n.1374T>A
|
|
|
ENST00000578809.5:n.393T>A
|
|
|
ENST00000579425.5:n.937T>A
|
|
|
ENST00000579546.1:c.556T>A
|
|
|
ENST00000583848.5:c.187T>A
|
ENSP00000466487.1:n.187T>A
|
|
ENST00000583850.5:n.592T>A
|
|
|
ENST00000583858.5:c.752T>A
|
|
|
NM_000018.3:c.1821T>A
|
NP_000009.1:p.Cys607Ter
|
|
NM_001033859.2:c.1755T>A
|
NP_001029031.1:p.Cys585Ter
|
|
NM_001270447.1:c.1890T>A
|
NP_001257376.1:p.Cys630Ter
|
|
NM_001270448.1:c.1593T>A
|
NP_001257377.1:p.Cys531Ter
|
|
XM_006721516.2:c.1842T>A
|
XP_006721579.2:p.Cys614Ter
|
|
XM_011523829.1:c.1740T>A
|
XP_011522131.1:p.Cys580Ter
|
|
XM_011523830.1:c.1719T>A
|
XP_011522132.1:p.Cys573Ter
|
|
XR_934021.1:n.1924T>A
|
|
|
XR_934022.1:n.1830T>A
|
|
|
XR_934023.1:n.1851T>A
|
|
|
XM_006721516.3:c.1842T>A
|
XP_006721579.2:p.Cys614Ter
|
|
XM_011523829.2:c.1740T>A
|
XP_011522131.1:p.Cys580Ter
|
|
XM_011523830.2:c.1719T>A
|
XP_011522132.1:p.Cys573Ter
|
|
XM_024450741.1:c.1809T>A
|
XP_024306509.1:p.Cys603Ter
|
|
XR_934021.2:n.1876T>A
|
|
|
XR_934022.2:n.1782T>A
|
|
|
XR_934023.2:n.1803T>A
|
|
|
NM_000018.4:c.1821T>A
MANE Select
|
NP_000009.1:p.Cys607Ter
|
|
NM_001033859.3:c.1755T>A
|
NP_001029031.1:p.Cys585Ter
|
|
NM_001270447.2:c.1890T>A
|
NP_001257376.1:p.Cys630Ter
|
|
NM_001270448.2:c.1593T>A
|
NP_001257377.1:p.Cys531Ter
|
|