ENST00000644991.3:c.669T>C
MANE Select
|
ENSP00000495607.1:p.Ser223=
|
|
ENST00000614701.4:c.669T>C
|
ENSP00000482885.1:p.Ser223=
|
|
ENST00000616559.4:c.795T>C
|
ENSP00000483259.1:p.Ser265=
|
|
NM_001145026.1:c.669T>C
|
NP_001138498.1:p.Ser223=
|
|
XM_011538290.1:c.669T>C
|
XP_011536592.1:p.Ser223=
|
|
XM_017019273.1:c.1335T>C
|
XP_016874762.1:p.Ser445=
|
|
XM_017019274.1:c.1335T>C
|
XP_016874763.1:p.Ser445=
|
|
XM_017019275.1:c.1335T>C
|
XP_016874764.1:p.Ser445=
|
|
XR_001748688.1:n.1472T>C
|
|
|
XR_001748689.1:n.1472T>C
|
|
|
NM_001145026.2:c.669T>C
MANE Select
|
NP_001138498.1:p.Ser223=
|
|