ENST00000253122.10:c.1365T>C
MANE Select
|
ENSP00000253122.5:p.Phe455=
|
|
ENST00000253122.9:c.1365T>C
|
ENSP00000253122.5:p.Phe455=
|
|
ENST00000413787.1:c.294T>C
|
ENSP00000400463.1:p.Phe98=
|
|
ENST00000430077.6:c.1020T>C
|
ENSP00000403041.2:p.Phe340=
|
|
ENST00000442457.1:c.419T>C
|
|
|
ENST00000485324.1:n.1510T>C
|
|
|
NM_001142805.1:c.1335T>C
|
NP_001136277.1:p.Phe445=
|
|
NM_001142806.1:c.1020T>C
|
NP_001136278.1:p.Phe340=
|
|
NM_005629.3:c.1365T>C
|
NP_005620.1:p.Phe455=
|
|
NM_005629.4:c.1365T>C
MANE Select
|
NP_005620.1:p.Phe455=
|
|
NM_001142805.2:c.1335T>C
|
NP_001136277.1:p.Phe445=
|
|