ENST00000368680.4:c.1484G>C
MANE Select
|
ENSP00000357669.3:p.Arg495Thr
|
|
ENST00000368680.3:c.1484G>C
|
ENSP00000357669.3:p.Arg495Thr
|
|
NM_000906.3:c.1484G>C
|
NP_000897.3:p.Arg495Thr
|
|
XM_005245218.1:c.1484G>C
|
XP_005245275.1:p.Arg495Thr
|
|
XM_006711342.1:c.1484G>C
|
XP_006711405.1:p.Arg495Thr
|
|
XM_006711343.1:c.1484G>C
|
XP_006711406.1:p.Arg495Thr
|
|
XM_011509585.1:c.1484G>C
|
XP_011507887.1:p.Arg495Thr
|
|
XM_005245218.2:c.1484G>C
|
XP_005245275.1:p.Arg495Thr
|
|
XM_017001374.2:c.1484G>C
|
XP_016856863.1:p.Arg495Thr
|
|
NM_000906.4:c.1484G>C
MANE Select
|
NP_000897.3:p.Arg495Thr
|
|