ENST00000460843.6:c.2895C>T
MANE Select
|
ENSP00000417980.1:p.Val965=
|
|
ENST00000636027.1:c.2781C>T
|
ENSP00000489961.1:p.Val927=
|
|
ENST00000637161.1:c.2802C>T
|
ENSP00000490328.1:p.Val934=
|
|
ENST00000637261.1:c.2935C>T
|
ENSP00000490815.1:n.2935C>T
|
|
ENST00000637891.1:c.789C>T
|
ENSP00000490907.1:p.Val263=
|
|
ENST00000460843.5:c.2895C>T
|
ENSP00000417980.1:p.Val965=
|
|
ENST00000462942.3:c.1752C>T
|
ENSP00000436107.1:p.Val584=
|
|
ENST00000486164.5:c.582C>T
|
|
|
ENST00000488242.2:n.421C>T
|
|
|
NM_024757.4:c.2895C>T
|
NP_079033.4:p.Val965=
|
|
XM_005266105.3:c.2886C>T
|
XP_005266162.1:p.Val962=
|
|
XM_005266110.1:c.2802C>T
|
XP_005266167.1:p.Val934=
|
|
XM_006717288.2:c.2877C>T
|
XP_006717351.1:p.Val959=
|
|
XM_011519021.1:c.2904C>T
|
XP_011517323.1:p.Val968=
|
|
XM_011519022.1:c.2901C>T
|
XP_011517324.1:p.Val967=
|
|
XM_011519023.1:c.2883C>T
|
XP_011517325.1:p.Val961=
|
|
XM_011519024.1:c.2826C>T
|
XP_011517326.1:p.Val942=
|
|
XM_011519025.1:c.2802C>T
|
XP_011517327.1:p.Val934=
|
|
XM_011519026.1:c.2760C>T
|
XP_011517328.1:p.Val920=
|
|
XM_011519029.1:c.1326C>T
|
XP_011517331.1:p.Val442=
|
|
XM_011519030.1:c.678C>T
|
XP_011517332.1:p.Val226=
|
|
XM_011519031.1:c.465C>T
|
XP_011517333.1:p.Val155=
|
|
XM_011519032.1:c.465C>T
|
XP_011517334.1:p.Val155=
|
|
XM_011519033.1:c.2739C>T
|
XP_011517335.1:p.Val913=
|
|
NM_001354263.1:c.2874C>T
|
NP_001341192.1:p.Val958=
|
|
XM_005266105.5:c.2886C>T
|
XP_005266162.1:p.Val962=
|
|
XM_011519021.3:c.2904C>T
|
XP_011517323.1:p.Val968=
|
|
XM_011519022.3:c.2901C>T
|
XP_011517324.1:p.Val967=
|
|
XM_011519023.3:c.2883C>T
|
XP_011517325.1:p.Val961=
|
|
XM_011519029.3:c.1326C>T
|
XP_011517331.1:p.Val442=
|
|
XM_011519030.3:c.678C>T
|
XP_011517332.1:p.Val226=
|
|
XM_017015134.1:c.2880C>T
|
XP_016870623.1:p.Val960=
|
|
XM_017015136.2:c.2796C>T
|
XP_016870625.1:p.Val932=
|
|
XM_017015137.1:c.2781C>T
|
XP_016870626.1:p.Val927=
|
|
XM_017015138.1:c.2781C>T
|
XP_016870627.1:p.Val927=
|
|
XM_024447674.1:c.2724C>T
|
XP_024303442.1:p.Val908=
|
|
XM_024447675.1:c.2658C>T
|
XP_024303443.1:p.Val886=
|
|
XM_024447676.1:c.2019C>T
|
XP_024303444.1:p.Val673=
|
|
XM_024447677.1:c.2019C>T
|
XP_024303445.1:p.Val673=
|
|
XM_024447680.1:c.2637C>T
|
XP_024303448.1:p.Val879=
|
|
NM_024757.5:c.2895C>T
MANE Select
|
NP_079033.4:p.Val965=
|
|
NM_001354263.2:c.2874C>T
|
NP_001341192.1:p.Val958=
|
|