ENST00000253122.10:c.1342G>T
MANE Select
|
ENSP00000253122.5:p.Ala448Ser
|
|
ENST00000253122.9:c.1342G>T
|
ENSP00000253122.5:p.Ala448Ser
|
|
ENST00000413787.1:c.271G>T
|
ENSP00000400463.1:p.Ala91Ser
|
|
ENST00000430077.6:c.997G>T
|
ENSP00000403041.2:p.Ala333Ser
|
|
ENST00000442457.1:c.396G>T
|
|
|
ENST00000485324.1:n.1487G>T
|
|
|
NM_001142805.1:c.1312G>T
|
NP_001136277.1:p.Ala438Ser
|
|
NM_001142806.1:c.997G>T
|
NP_001136278.1:p.Ala333Ser
|
|
NM_005629.3:c.1342G>T
|
NP_005620.1:p.Ala448Ser
|
|
NM_005629.4:c.1342G>T
MANE Select
|
NP_005620.1:p.Ala448Ser
|
|
NM_001142805.2:c.1312G>T
|
NP_001136277.1:p.Ala438Ser
|
|