ENST00000272371.7:c.5939C>T
MANE Select
|
ENSP00000272371.2:p.Ala1980Val
|
|
ENST00000339598.8:c.3512+567C>T
MANE Plus Clinical
|
ENSP00000344521.3:n.3512+567C>T
|
|
ENST00000402415.8:c.3698C>T
|
ENSP00000383906.4:p.Ala1233Val
|
|
ENST00000272371.6:c.5939C>T
|
ENSP00000272371.2:p.Ala1980Val
|
|
ENST00000338581.10:c.3638C>T
|
ENSP00000345137.6:p.Ala1213Val
|
|
ENST00000339598.7:c.3512+567C>T
|
ENSP00000344521.3:n.3512+567C>T
|
|
ENST00000402415.7:c.3869C>T
|
ENSP00000383906.3:p.Ala1290Val
|
|
ENST00000403946.7:c.5813+567C>T
|
ENSP00000385255.3:n.5813+567C>T
|
|
NM_001287489.1:c.5813+567C>T
|
NP_001274418.1:n.5813+567C>T
|
|
NM_004802.3:c.3638C>T
|
NP_004793.2:p.Ala1213Val
|
|
NM_194248.2:c.5939C>T
|
NP_919224.1:p.Ala1980Val
|
|
NM_194322.2:c.3869C>T
|
NP_919303.1:p.Ala1290Val
|
|
NM_194323.2:c.3512+567C>T
|
NP_919304.1:n.3512+567C>T
|
|
XM_005264644.2:c.5798+567C>T
|
XP_005264701.1:n.5798+567C>T
|
|
XM_011533185.1:c.5858+567C>T
|
XP_011531487.1:n.5858+567C>T
|
|
XM_017005338.1:c.5879C>T
|
XP_016860827.1:p.Ala1960Val
|
|
NM_001287489.2:c.5813+567C>T
|
NP_001274418.1:n.5813+567C>T
|
|
NM_004802.4:c.3638C>T
|
NP_004793.2:p.Ala1213Val
|
|
NM_194248.3:c.5939C>T
MANE Select
|
NP_919224.1:p.Ala1980Val
|
|
NM_194322.3:c.3869C>T
|
NP_919303.1:p.Ala1290Val
|
|
NM_194323.3:c.3512+567C>T
MANE Plus Clinical
|
NP_919304.1:n.3512+567C>T
|
|