ENST00000460843.6:c.3501T=
MANE Select
|
ENSP00000417980.1:p.Val1167=
|
|
ENST00000636472.1:n.63T=
|
|
|
ENST00000637161.1:c.3408T=
|
ENSP00000490328.1:p.Val1136=
|
|
ENST00000637261.1:c.4075T=
|
ENSP00000490815.1:n.4075T=
|
|
ENST00000637748.1:n.482T=
|
|
|
ENST00000637891.1:c.1575T=
|
ENSP00000490907.1:n.1575T=
|
|
ENST00000460843.5:c.3501T=
|
ENSP00000417980.1:p.Val1167=
|
|
ENST00000462942.3:c.2358T=
|
ENSP00000436107.1:p.Val786=
|
|
ENST00000475564.5:n.1225T=
|
|
|
ENST00000494249.5:n.854T=
|
|
|
NM_024757.4:c.3501T=
|
NP_079033.4:p.Val1167=
|
|
XM_005266105.3:c.3492T=
|
XP_005266162.1:p.Val1164=
|
|
XM_005266110.1:c.3408T=
|
XP_005266167.1:p.Val1136=
|
|
XM_006717288.2:c.3483T=
|
XP_006717351.1:p.Val1161=
|
|
XM_011519021.1:c.3510T=
|
XP_011517323.1:p.Val1170=
|
|
XM_011519022.1:c.3507T=
|
XP_011517324.1:p.Val1169=
|
|
XM_011519023.1:c.3489T=
|
XP_011517325.1:p.Val1163=
|
|
XM_011519024.1:c.3432T=
|
XP_011517326.1:p.Val1144=
|
|
XM_011519025.1:c.3408T=
|
XP_011517327.1:p.Val1136=
|
|
XM_011519026.1:c.3366T=
|
XP_011517328.1:p.Val1122=
|
|
XM_011519029.1:c.1932T=
|
XP_011517331.1:p.Val644=
|
|
XM_011519030.1:c.1284T=
|
XP_011517332.1:p.Val428=
|
|
XM_011519031.1:c.1071T=
|
XP_011517333.1:p.Val357=
|
|
XM_011519032.1:c.1071T=
|
XP_011517334.1:p.Val357=
|
|
XM_011519033.1:c.3345T=
|
XP_011517335.1:p.Val1115=
|
|
XR_930459.1:n.5297-3537A=
|
|
|
NM_001354263.1:c.3480T=
|
NP_001341192.1:p.Val1160=
|
|
XM_005266105.5:c.3492T=
|
XP_005266162.1:p.Val1164=
|
|
XM_011519021.3:c.3510T=
|
XP_011517323.1:p.Val1170=
|
|
XM_011519022.3:c.3507T=
|
XP_011517324.1:p.Val1169=
|
|
XM_011519023.3:c.3489T=
|
XP_011517325.1:p.Val1163=
|
|
XM_011519029.3:c.1932T=
|
XP_011517331.1:p.Val644=
|
|
XM_011519030.3:c.1284T=
|
XP_011517332.1:p.Val428=
|
|
XM_017015134.1:c.3486T=
|
XP_016870623.1:p.Val1162=
|
|
XM_017015136.2:c.3402T=
|
XP_016870625.1:p.Val1134=
|
|
XM_017015137.1:c.3387T=
|
XP_016870626.1:p.Val1129=
|
|
XM_017015138.1:c.3387T=
|
XP_016870627.1:p.Val1129=
|
|
XM_024447674.1:c.3330T=
|
XP_024303442.1:p.Val1110=
|
|
XM_024447675.1:c.3264T=
|
XP_024303443.1:p.Val1088=
|
|
XM_024447676.1:c.2625T=
|
XP_024303444.1:p.Val875=
|
|
XM_024447677.1:c.2625T=
|
XP_024303445.1:p.Val875=
|
|
XM_024447680.1:c.3243T=
|
XP_024303448.1:p.Val1081=
|
|
NM_024757.5:c.3501T=
MANE Select
|
NP_079033.4:p.Val1167=
|
|
NM_001354263.2:c.3480T=
|
NP_001341192.1:p.Val1160=
|
|