ENST00000460843.6:c.2879C>T
MANE Select
|
ENSP00000417980.1:p.Ser960Phe
|
|
ENST00000636027.1:c.2765C>T
|
ENSP00000489961.1:p.Ser922Phe
|
|
ENST00000637161.1:c.2786C>T
|
ENSP00000490328.1:p.Ser929Phe
|
|
ENST00000637261.1:c.2919C>T
|
ENSP00000490815.1:n.2919C>T
|
|
ENST00000637891.1:c.773C>T
|
ENSP00000490907.1:p.Ser258Phe
|
|
ENST00000460843.5:c.2879C>T
|
ENSP00000417980.1:p.Ser960Phe
|
|
ENST00000462942.3:c.1736C>T
|
ENSP00000436107.1:p.Ser579Phe
|
|
ENST00000486164.5:c.566C>T
|
|
|
ENST00000488242.2:n.405C>T
|
|
|
NM_024757.4:c.2879C>T
|
NP_079033.4:p.Ser960Phe
|
|
XM_005266105.3:c.2870C>T
|
XP_005266162.1:p.Ser957Phe
|
|
XM_005266110.1:c.2786C>T
|
XP_005266167.1:p.Ser929Phe
|
|
XM_006717288.2:c.2861C>T
|
XP_006717351.1:p.Ser954Phe
|
|
XM_011519021.1:c.2888C>T
|
XP_011517323.1:p.Ser963Phe
|
|
XM_011519022.1:c.2885C>T
|
XP_011517324.1:p.Ser962Phe
|
|
XM_011519023.1:c.2867C>T
|
XP_011517325.1:p.Ser956Phe
|
|
XM_011519024.1:c.2810C>T
|
XP_011517326.1:p.Ser937Phe
|
|
XM_011519025.1:c.2786C>T
|
XP_011517327.1:p.Ser929Phe
|
|
XM_011519026.1:c.2744C>T
|
XP_011517328.1:p.Ser915Phe
|
|
XM_011519029.1:c.1310C>T
|
XP_011517331.1:p.Ser437Phe
|
|
XM_011519030.1:c.662C>T
|
XP_011517332.1:p.Ser221Phe
|
|
XM_011519031.1:c.449C>T
|
XP_011517333.1:p.Ser150Phe
|
|
XM_011519032.1:c.449C>T
|
XP_011517334.1:p.Ser150Phe
|
|
XM_011519033.1:c.2723C>T
|
XP_011517335.1:p.Ser908Phe
|
|
NM_001354263.1:c.2858C>T
|
NP_001341192.1:p.Ser953Phe
|
|
XM_005266105.5:c.2870C>T
|
XP_005266162.1:p.Ser957Phe
|
|
XM_011519021.3:c.2888C>T
|
XP_011517323.1:p.Ser963Phe
|
|
XM_011519022.3:c.2885C>T
|
XP_011517324.1:p.Ser962Phe
|
|
XM_011519023.3:c.2867C>T
|
XP_011517325.1:p.Ser956Phe
|
|
XM_011519029.3:c.1310C>T
|
XP_011517331.1:p.Ser437Phe
|
|
XM_011519030.3:c.662C>T
|
XP_011517332.1:p.Ser221Phe
|
|
XM_017015134.1:c.2864C>T
|
XP_016870623.1:p.Ser955Phe
|
|
XM_017015136.2:c.2780C>T
|
XP_016870625.1:p.Ser927Phe
|
|
XM_017015137.1:c.2765C>T
|
XP_016870626.1:p.Ser922Phe
|
|
XM_017015138.1:c.2765C>T
|
XP_016870627.1:p.Ser922Phe
|
|
XM_024447674.1:c.2708C>T
|
XP_024303442.1:p.Ser903Phe
|
|
XM_024447675.1:c.2642C>T
|
XP_024303443.1:p.Ser881Phe
|
|
XM_024447676.1:c.2003C>T
|
XP_024303444.1:p.Ser668Phe
|
|
XM_024447677.1:c.2003C>T
|
XP_024303445.1:p.Ser668Phe
|
|
XM_024447680.1:c.2621C>T
|
XP_024303448.1:p.Ser874Phe
|
|
NM_024757.5:c.2879C>T
MANE Select
|
NP_079033.4:p.Ser960Phe
|
|
NM_001354263.2:c.2858C>T
|
NP_001341192.1:p.Ser953Phe
|
|