ENST00000359271.4:c.434T>C
MANE Select
|
ENSP00000352216.2:p.Val145Ala
|
|
ENST00000359271.3:c.434T>C
|
ENSP00000352216.2:p.Val145Ala
|
|
ENST00000611837.1:n.586T>C
|
|
|
NM_030777.3:c.434T>C
|
NP_110404.1:p.Val145Ala
|
|
XM_011529060.1:c.497T>C
|
XP_011527362.1:p.Val166Ala
|
|
XM_011529061.1:c.443T>C
|
XP_011527363.1:p.Val148Ala
|
|
XM_011529062.1:c.497T>C
|
XP_011527364.1:p.Val166Ala
|
|
XM_011529063.1:c.497T>C
|
XP_011527365.1:p.Val166Ala
|
|
XM_011529064.1:c.497T>C
|
XP_011527366.1:p.Val166Ala
|
|
XM_011529065.1:c.497T>C
|
XP_011527367.1:p.Val166Ala
|
|
XR_936641.1:n.633T>C
|
|
|
XM_011529060.2:c.497T>C
|
XP_011527362.1:p.Val166Ala
|
|
XM_011529061.2:c.443T>C
|
XP_011527363.1:p.Val148Ala
|
|
XM_011529062.2:c.497T>C
|
XP_011527364.1:p.Val166Ala
|
|
XM_011529063.2:c.497T>C
|
XP_011527365.1:p.Val166Ala
|
|
XM_011529064.2:c.497T>C
|
XP_011527366.1:p.Val166Ala
|
|
XM_011529065.2:c.497T>C
|
XP_011527367.1:p.Val166Ala
|
|
XM_017028087.2:c.434T>C
|
XP_016883576.1:p.Val145Ala
|
|
XR_936641.2:n.620T>C
|
|
|
NM_030777.4:c.434T>C
MANE Select
|
NP_110404.1:p.Val145Ala
|
|