ENST00000460843.6:c.3016G=
MANE Select
|
ENSP00000417980.1:p.Val1006=
|
|
ENST00000636027.1:c.2902G=
|
ENSP00000489961.1:p.Val968=
|
|
ENST00000637161.1:c.2923G=
|
ENSP00000490328.1:p.Val975=
|
|
ENST00000637261.1:c.3056G=
|
ENSP00000490815.1:n.3056G=
|
|
ENST00000637891.1:c.910G=
|
ENSP00000490907.1:p.Val304=
|
|
ENST00000460843.5:c.3016G=
|
ENSP00000417980.1:p.Val1006=
|
|
ENST00000462942.3:c.1873G=
|
ENSP00000436107.1:p.Val625=
|
|
ENST00000486164.5:c.703G=
|
|
|
ENST00000488242.2:n.542G=
|
|
|
NM_024757.4:c.3016G=
|
NP_079033.4:p.Val1006=
|
|
XM_005266105.3:c.3007G=
|
XP_005266162.1:p.Val1003=
|
|
XM_005266110.1:c.2923G=
|
XP_005266167.1:p.Val975=
|
|
XM_006717288.2:c.2998G=
|
XP_006717351.1:p.Val1000=
|
|
XM_011519021.1:c.3025G=
|
XP_011517323.1:p.Val1009=
|
|
XM_011519022.1:c.3022G=
|
XP_011517324.1:p.Val1008=
|
|
XM_011519023.1:c.3004G=
|
XP_011517325.1:p.Val1002=
|
|
XM_011519024.1:c.2947G=
|
XP_011517326.1:p.Val983=
|
|
XM_011519025.1:c.2923G=
|
XP_011517327.1:p.Val975=
|
|
XM_011519026.1:c.2881G=
|
XP_011517328.1:p.Val961=
|
|
XM_011519029.1:c.1447G=
|
XP_011517331.1:p.Val483=
|
|
XM_011519030.1:c.799G=
|
XP_011517332.1:p.Val267=
|
|
XM_011519031.1:c.586G=
|
XP_011517333.1:p.Val196=
|
|
XM_011519032.1:c.586G=
|
XP_011517334.1:p.Val196=
|
|
XM_011519033.1:c.2860G=
|
XP_011517335.1:p.Val954=
|
|
NM_001354263.1:c.2995G=
|
NP_001341192.1:p.Val999=
|
|
XM_005266105.5:c.3007G=
|
XP_005266162.1:p.Val1003=
|
|
XM_011519021.3:c.3025G=
|
XP_011517323.1:p.Val1009=
|
|
XM_011519022.3:c.3022G=
|
XP_011517324.1:p.Val1008=
|
|
XM_011519023.3:c.3004G=
|
XP_011517325.1:p.Val1002=
|
|
XM_011519029.3:c.1447G=
|
XP_011517331.1:p.Val483=
|
|
XM_011519030.3:c.799G=
|
XP_011517332.1:p.Val267=
|
|
XM_017015134.1:c.3001G=
|
XP_016870623.1:p.Val1001=
|
|
XM_017015136.2:c.2917G=
|
XP_016870625.1:p.Val973=
|
|
XM_017015137.1:c.2902G=
|
XP_016870626.1:p.Val968=
|
|
XM_017015138.1:c.2902G=
|
XP_016870627.1:p.Val968=
|
|
XM_024447674.1:c.2845G=
|
XP_024303442.1:p.Val949=
|
|
XM_024447675.1:c.2779G=
|
XP_024303443.1:p.Val927=
|
|
XM_024447676.1:c.2140G=
|
XP_024303444.1:p.Val714=
|
|
XM_024447677.1:c.2140G=
|
XP_024303445.1:p.Val714=
|
|
XM_024447680.1:c.2758G=
|
XP_024303448.1:p.Val920=
|
|
NM_024757.5:c.3016G=
MANE Select
|
NP_079033.4:p.Val1006=
|
|
NM_001354263.2:c.2995G=
|
NP_001341192.1:p.Val999=
|
|