ENST00000512123.4:c.10820C>G
MANE Select
|
ENSP00000422834.2:p.Ser3607Ter
|
|
ENST00000512123.3:c.10820C>G
|
ENSP00000422834.2:p.Ser3607Ter
|
|
NM_025074.6:c.10820C>G
|
NP_079350.5:p.Ser3607Ter
|
|
XM_006714314.1:c.10814C>G
|
XP_006714377.1:p.Ser3605Ter
|
|
XM_006714316.1:c.10592C>G
|
XP_006714379.1:p.Ser3531Ter
|
|
XM_011532270.1:c.8519C>G
|
XP_011530572.1:p.Ser2840Ter
|
|
XM_011532271.1:c.5708C>G
|
XP_011530573.1:p.Ser1903Ter
|
|
XM_006714316.3:c.10592C>G
|
XP_006714379.1:p.Ser3531Ter
|
|
NM_025074.7:c.10820C>G
MANE Select
|
NP_079350.5:p.Ser3607Ter
|
|