ENST00000367400.8:c.4033T>G
MANE Select
|
ENSP00000356370.3:p.Phe1345Val
|
|
ENST00000367399.6:c.3697T>G
|
ENSP00000356369.2:p.Phe1233Val
|
|
ENST00000367400.7:c.4033T>G
|
ENSP00000356370.3:p.Phe1345Val
|
|
ENST00000448952.1:c.267T>G
|
ENSP00000395407.1:n.267T>G
|
|
ENST00000484075.5:c.*144T>G
|
ENSP00000433932.1:n.*144T>G
|
|
ENST00000535699.5:c.3961T>G
|
ENSP00000438786.1:p.Phe1321Val
|
|
ENST00000538660.5:c.2425T>G
|
ENSP00000438091.1:p.Phe809Val
|
|
NM_001193640.1:c.3697T>G
|
NP_001180569.1:p.Phe1233Val
|
|
NM_001257965.1:c.3961T>G
|
NP_001244894.1:p.Phe1321Val
|
|
NM_001257966.1:c.2425T>G
|
NP_001244895.1:p.Phe809Val
|
|
NM_201253.2:c.4033T>G
|
NP_957705.1:p.Phe1345Val
|
|
NR_047563.1:n.4034T>G
|
|
|
NR_047564.1:n.4484T>G
|
|
|
XM_011509366.1:c.*138T>G
|
XP_011507668.1:n.*138T>G
|
|
XM_011509367.1:c.*12T>G
|
XP_011507669.1:n.*12T>G
|
|
XM_011509368.1:c.3451T>G
|
XP_011507670.1:p.Phe1151Val
|
|
XM_011509369.1:c.2476T>G
|
XP_011507671.1:p.Phe826Val
|
|
XM_011509369.2:c.2476T>G
|
XP_011507671.1:p.Phe826Val
|
|
XM_017000851.1:c.3190T>G
|
XP_016856340.1:p.Phe1064Val
|
|
XM_017000852.1:c.4168T>G
|
XP_016856341.1:p.Phe1390Val
|
|
NM_201253.3:c.4033T>G
MANE Select
|
NP_957705.1:p.Phe1345Val
|
|
NM_001193640.2:c.3697T>G
|
NP_001180569.1:p.Phe1233Val
|
|
NM_001257965.2:c.3961T>G
|
NP_001244894.1:p.Phe1321Val
|
|
NR_047563.2:n.3986T>G
|
|
|
NR_047564.2:n.4436T>G
|
|
|
NM_001257966.2:c.2425T>G
|
NP_001244895.1:p.Phe809Val
|
|