|
NM_025074.7:c.8940A>G
MANE Select
|
NP_079350.5:p.Thr2980=
|
|
ENST00000512123.4:c.8940A>G
MANE Select
|
ENSP00000422834.2:p.Thr2980=
|
|
NM_025074.6:c.8940A>G
|
NP_079350.5:p.Thr2980=
|
|
ENST00000512123.3:c.8940A>G
|
ENSP00000422834.2:p.Thr2980=
|
|
ENST00000682513.1:c.8940A>G
|
ENSP00000508201.1:p.Thr2980=
|
|
XM_006714314.1:c.8934A>G
|
XP_006714377.1:p.Thr2978=
|
|
XM_006714316.1:c.8712A>G
|
XP_006714379.1:p.Thr2904=
|
|
XM_006714316.3:c.8712A>G
|
XP_006714379.1:p.Thr2904=
|
|
XM_011532270.1:c.6639A>G
|
XP_011530572.1:p.Thr2213=
|
|
XM_011532271.1:c.3828A>G
|
XP_011530573.1:p.Thr1276=
|