ENST00000599672.6:c.179C>G
MANE Select
|
ENSP00000470560.1:p.Thr60Arg
|
|
ENST00000261406.7:c.161C>G
|
ENSP00000476966.2:p.Thr54Arg
|
|
ENST00000539196.2:c.42C>G
|
|
|
ENST00000599672.5:c.179C>G
|
ENSP00000470560.1:p.Thr60Arg
|
|
ENST00000607161.5:c.182C>G
|
ENSP00000480420.1:p.Thr61Arg
|
|
ENST00000611981.1:n.190C>G
|
|
|
ENST00000620255.1:n.168C>G
|
|
|
NM_006331.7:c.179C>G
|
NP_006322.4:p.Thr60Arg
|
|
XM_011520907.1:c.179C>G
|
XP_011519209.1:p.Thr60Arg
|
|
NM_001320049.1:c.179C>G
|
NP_001306978.1:p.Thr60Arg
|
|
NR_135131.1:n.322C>G
|
|
|
NM_006331.8:c.179C>G
MANE Select
|
NP_006322.4:p.Thr60Arg
|
|
NM_001320049.2:c.179C>G
|
NP_001306978.1:p.Thr60Arg
|
|
NR_135131.2:n.190C>G
|
|
|