ENST00000696290.1:c.2606T>C
MANE Select
|
ENSP00000512529.1:p.Met869Thr
|
|
ENST00000155858.10:c.2606T>C
|
ENSP00000155858.5:p.Met869Thr
|
|
ENST00000528453.1:c.2606T>C
|
ENSP00000436809.1:p.Met869Thr
|
|
ENST00000533060.5:c.2606T>C
|
ENSP00000434121.1:p.Met869Thr
|
|
ENST00000533881.5:c.2588T>C
|
ENSP00000434383.1:p.Met863Thr
|
|
NM_014555.3:c.2606T>C
|
NP_055370.1:p.Met869Thr
|
|
XM_011520035.1:c.2867T>C
|
XP_011518337.1:p.Met956Thr
|
|
XM_017017628.1:c.2660T>C
|
XP_016873117.1:p.Met887Thr
|
|
NM_014555.4:c.2606T>C
MANE Select
|
NP_055370.1:p.Met869Thr
|
|