ENST00000460843.6:c.2939G>C
MANE Select
|
ENSP00000417980.1:p.Ser980Thr
|
|
ENST00000636027.1:c.2825G>C
|
ENSP00000489961.1:p.Ser942Thr
|
|
ENST00000637161.1:c.2846G>C
|
ENSP00000490328.1:p.Ser949Thr
|
|
ENST00000637261.1:c.2979G>C
|
ENSP00000490815.1:n.2979G>C
|
|
ENST00000637891.1:c.833G>C
|
ENSP00000490907.1:p.Ser278Thr
|
|
ENST00000460843.5:c.2939G>C
|
ENSP00000417980.1:p.Ser980Thr
|
|
ENST00000462942.3:c.1796G>C
|
ENSP00000436107.1:p.Ser599Thr
|
|
ENST00000486164.5:c.626G>C
|
|
|
ENST00000488242.2:n.465G>C
|
|
|
NM_024757.4:c.2939G>C
|
NP_079033.4:p.Ser980Thr
|
|
XM_005266105.3:c.2930G>C
|
XP_005266162.1:p.Ser977Thr
|
|
XM_005266110.1:c.2846G>C
|
XP_005266167.1:p.Ser949Thr
|
|
XM_006717288.2:c.2921G>C
|
XP_006717351.1:p.Ser974Thr
|
|
XM_011519021.1:c.2948G>C
|
XP_011517323.1:p.Ser983Thr
|
|
XM_011519022.1:c.2945G>C
|
XP_011517324.1:p.Ser982Thr
|
|
XM_011519023.1:c.2927G>C
|
XP_011517325.1:p.Ser976Thr
|
|
XM_011519024.1:c.2870G>C
|
XP_011517326.1:p.Ser957Thr
|
|
XM_011519025.1:c.2846G>C
|
XP_011517327.1:p.Ser949Thr
|
|
XM_011519026.1:c.2804G>C
|
XP_011517328.1:p.Ser935Thr
|
|
XM_011519029.1:c.1370G>C
|
XP_011517331.1:p.Ser457Thr
|
|
XM_011519030.1:c.722G>C
|
XP_011517332.1:p.Ser241Thr
|
|
XM_011519031.1:c.509G>C
|
XP_011517333.1:p.Ser170Thr
|
|
XM_011519032.1:c.509G>C
|
XP_011517334.1:p.Ser170Thr
|
|
XM_011519033.1:c.2783G>C
|
XP_011517335.1:p.Ser928Thr
|
|
NM_001354263.1:c.2918G>C
|
NP_001341192.1:p.Ser973Thr
|
|
XM_005266105.5:c.2930G>C
|
XP_005266162.1:p.Ser977Thr
|
|
XM_011519021.3:c.2948G>C
|
XP_011517323.1:p.Ser983Thr
|
|
XM_011519022.3:c.2945G>C
|
XP_011517324.1:p.Ser982Thr
|
|
XM_011519023.3:c.2927G>C
|
XP_011517325.1:p.Ser976Thr
|
|
XM_011519029.3:c.1370G>C
|
XP_011517331.1:p.Ser457Thr
|
|
XM_011519030.3:c.722G>C
|
XP_011517332.1:p.Ser241Thr
|
|
XM_017015134.1:c.2924G>C
|
XP_016870623.1:p.Ser975Thr
|
|
XM_017015136.2:c.2840G>C
|
XP_016870625.1:p.Ser947Thr
|
|
XM_017015137.1:c.2825G>C
|
XP_016870626.1:p.Ser942Thr
|
|
XM_017015138.1:c.2825G>C
|
XP_016870627.1:p.Ser942Thr
|
|
XM_024447674.1:c.2768G>C
|
XP_024303442.1:p.Ser923Thr
|
|
XM_024447675.1:c.2702G>C
|
XP_024303443.1:p.Ser901Thr
|
|
XM_024447676.1:c.2063G>C
|
XP_024303444.1:p.Ser688Thr
|
|
XM_024447677.1:c.2063G>C
|
XP_024303445.1:p.Ser688Thr
|
|
XM_024447680.1:c.2681G>C
|
XP_024303448.1:p.Ser894Thr
|
|
NM_024757.5:c.2939G>C
MANE Select
|
NP_079033.4:p.Ser980Thr
|
|
NM_001354263.2:c.2918G>C
|
NP_001341192.1:p.Ser973Thr
|
|