ENST00000216714.8:c.696C>T
MANE Select
|
ENSP00000216714.3:p.Phe232=
|
|
ENST00000216714.7:c.696C>T
|
ENSP00000216714.3:p.Phe232=
|
|
ENST00000398030.8:c.696C>T
|
ENSP00000381111.4:p.Phe232=
|
|
ENST00000553555.5:n.1116C>T
|
|
|
ENST00000553681.5:c.696C>T
|
ENSP00000451327.1:p.Phe232=
|
|
ENST00000555414.5:c.696C>T
|
ENSP00000451979.1:p.Phe232=
|
|
ENST00000555839.5:c.609C>T
|
ENSP00000452460.1:p.Phe203=
|
|
ENST00000557054.1:c.*107C>T
|
ENSP00000452212.2:n.*107C>T
|
|
ENST00000557159.5:n.1312C>T
|
|
|
ENST00000557365.1:n.776C>T
|
|
|
NM_001244249.1:c.696C>T
|
NP_001231178.1:p.Phe232=
|
|
NM_001641.3:c.696C>T
|
NP_001632.2:p.Phe232=
|
|
NM_080648.2:c.696C>T
|
NP_542379.1:p.Phe232=
|
|
NM_080649.2:c.696C>T
|
NP_542380.1:p.Phe232=
|
|
XM_005267581.3:c.696C>T
|
XP_005267638.1:p.Phe232=
|
|
XM_005267582.3:c.645C>T
|
XP_005267639.1:p.Phe215=
|
|
NM_001641.4:c.696C>T
MANE Select
|
NP_001632.2:p.Phe232=
|
|
NM_001244249.2:c.696C>T
|
NP_001231178.1:p.Phe232=
|
|
NM_080648.3:c.696C>T
|
NP_542379.1:p.Phe232=
|
|
NM_080649.3:c.696C>T
|
NP_542380.1:p.Phe232=
|
|