ENST00000456935.7:c.1511G>C
MANE Select
|
ENSP00000395473.2:p.Ser504Thr
|
|
ENST00000221363.8:c.1508G>C
|
ENSP00000221363.4:p.Ser503Thr
|
|
ENST00000433513.5:n.117G>C
|
|
|
ENST00000456935.6:c.1511G>C
|
ENSP00000395473.2:p.Ser504Thr
|
|
ENST00000466794.5:n.1410G>C
|
|
|
ENST00000495617.1:n.687G>C
|
|
|
ENST00000593686.1:c.121G>C
|
|
|
ENST00000595880.5:n.108G>C
|
|
|
NM_000528.3:c.1511G>C
|
NP_000519.2:p.Ser504Thr
|
|
NM_001173498.1:c.1508G>C
|
NP_001166969.1:p.Ser503Thr
|
|
XM_005259913.1:c.1514G>C
|
XP_005259970.1:p.Ser505Thr
|
|
XM_011528017.1:c.410G>C
|
XP_011526319.1:p.Ser137Thr
|
|
XM_005259913.2:c.1514G>C
|
XP_005259970.1:p.Ser505Thr
|
|
XM_024451518.1:c.410G>C
|
XP_024307286.1:p.Ser137Thr
|
|
NM_000528.4:c.1511G>C
MANE Select
|
NP_000519.2:p.Ser504Thr
|
|
NM_001173498.2:c.1508G>C
|
NP_001166969.1:p.Ser503Thr
|
|