|
NM_025074.7:c.8844C>T
MANE Select
|
NP_079350.5:p.Ser2948=
|
|
ENST00000512123.4:c.8844C>T
MANE Select
|
ENSP00000422834.2:p.Ser2948=
|
|
NM_025074.6:c.8844C>T
|
NP_079350.5:p.Ser2948=
|
|
ENST00000512123.3:c.8844C>T
|
ENSP00000422834.2:p.Ser2948=
|
|
ENST00000682513.1:c.8844C>T
|
ENSP00000508201.1:p.Ser2948=
|
|
XM_006714314.1:c.8838C>T
|
XP_006714377.1:p.Ser2946=
|
|
XM_006714316.1:c.8616C>T
|
XP_006714379.1:p.Ser2872=
|
|
XM_006714316.3:c.8616C>T
|
XP_006714379.1:p.Ser2872=
|
|
XM_011532270.1:c.6543C>T
|
XP_011530572.1:p.Ser2181=
|
|
XM_011532271.1:c.3732C>T
|
XP_011530573.1:p.Ser1244=
|