ENST00000231749.8:c.585A>C
MANE Select
|
ENSP00000231749.3:p.Thr195=
|
|
ENST00000231749.7:c.585A>C
|
ENSP00000231749.3:p.Thr195=
|
|
ENST00000360165.7:c.585A>C
|
ENSP00000353289.3:p.Thr195=
|
|
ENST00000442887.1:c.456A>C
|
ENSP00000393687.1:p.Thr152=
|
|
ENST00000443080.5:c.*337A>C
|
ENSP00000415661.1:n.*337A>C
|
|
ENST00000475688.1:n.37A>C
|
|
|
NM_001308379.1:c.585A>C
|
NP_001295308.1:p.Thr195=
|
|
NM_015896.2:c.585A>C
|
NP_056980.2:p.Thr195=
|
|
NM_015896.3:c.585A>C
|
NP_056980.2:p.Thr195=
|
|
XM_005265216.2:c.348A>C
|
XP_005265273.1:p.Thr116=
|
|
XM_005265216.3:c.348A>C
|
XP_005265273.1:p.Thr116=
|
|
NM_015896.4:c.585A>C
MANE Select
|
NP_056980.2:p.Thr195=
|
|
NM_001308379.2:c.585A>C
|
NP_001295308.1:p.Thr195=
|
|