ENST00000460843.6:c.2880T=
MANE Select
|
ENSP00000417980.1:p.Ser960=
|
|
ENST00000636027.1:c.2766T=
|
ENSP00000489961.1:p.Ser922=
|
|
ENST00000637161.1:c.2787T=
|
ENSP00000490328.1:p.Ser929=
|
|
ENST00000637261.1:c.2920T=
|
ENSP00000490815.1:n.2920T=
|
|
ENST00000637891.1:c.774T=
|
ENSP00000490907.1:p.Ser258=
|
|
ENST00000460843.5:c.2880T=
|
ENSP00000417980.1:p.Ser960=
|
|
ENST00000462942.3:c.1737T=
|
ENSP00000436107.1:p.Ser579=
|
|
ENST00000486164.5:c.567T=
|
|
|
ENST00000488242.2:n.406T=
|
|
|
NM_024757.4:c.2880T=
|
NP_079033.4:p.Ser960=
|
|
XM_005266105.3:c.2871T=
|
XP_005266162.1:p.Ser957=
|
|
XM_005266110.1:c.2787T=
|
XP_005266167.1:p.Ser929=
|
|
XM_006717288.2:c.2862T=
|
XP_006717351.1:p.Ser954=
|
|
XM_011519021.1:c.2889T=
|
XP_011517323.1:p.Ser963=
|
|
XM_011519022.1:c.2886T=
|
XP_011517324.1:p.Ser962=
|
|
XM_011519023.1:c.2868T=
|
XP_011517325.1:p.Ser956=
|
|
XM_011519024.1:c.2811T=
|
XP_011517326.1:p.Ser937=
|
|
XM_011519025.1:c.2787T=
|
XP_011517327.1:p.Ser929=
|
|
XM_011519026.1:c.2745T=
|
XP_011517328.1:p.Ser915=
|
|
XM_011519029.1:c.1311T=
|
XP_011517331.1:p.Ser437=
|
|
XM_011519030.1:c.663T=
|
XP_011517332.1:p.Ser221=
|
|
XM_011519031.1:c.450T=
|
XP_011517333.1:p.Ser150=
|
|
XM_011519032.1:c.450T=
|
XP_011517334.1:p.Ser150=
|
|
XM_011519033.1:c.2724T=
|
XP_011517335.1:p.Ser908=
|
|
NM_001354263.1:c.2859T=
|
NP_001341192.1:p.Ser953=
|
|
XM_005266105.5:c.2871T=
|
XP_005266162.1:p.Ser957=
|
|
XM_011519021.3:c.2889T=
|
XP_011517323.1:p.Ser963=
|
|
XM_011519022.3:c.2886T=
|
XP_011517324.1:p.Ser962=
|
|
XM_011519023.3:c.2868T=
|
XP_011517325.1:p.Ser956=
|
|
XM_011519029.3:c.1311T=
|
XP_011517331.1:p.Ser437=
|
|
XM_011519030.3:c.663T=
|
XP_011517332.1:p.Ser221=
|
|
XM_017015134.1:c.2865T=
|
XP_016870623.1:p.Ser955=
|
|
XM_017015136.2:c.2781T=
|
XP_016870625.1:p.Ser927=
|
|
XM_017015137.1:c.2766T=
|
XP_016870626.1:p.Ser922=
|
|
XM_017015138.1:c.2766T=
|
XP_016870627.1:p.Ser922=
|
|
XM_024447674.1:c.2709T=
|
XP_024303442.1:p.Ser903=
|
|
XM_024447675.1:c.2643T=
|
XP_024303443.1:p.Ser881=
|
|
XM_024447676.1:c.2004T=
|
XP_024303444.1:p.Ser668=
|
|
XM_024447677.1:c.2004T=
|
XP_024303445.1:p.Ser668=
|
|
XM_024447680.1:c.2622T=
|
XP_024303448.1:p.Ser874=
|
|
NM_024757.5:c.2880T=
MANE Select
|
NP_079033.4:p.Ser960=
|
|
NM_001354263.2:c.2859T=
|
NP_001341192.1:p.Ser953=
|
|