ENST00000319562.11:c.620C>G
MANE Select
|
ENSP00000322926.6:p.Thr207Arg
|
|
ENST00000596580.2:c.620C>G
|
ENSP00000490391.1:p.Thr207Arg
|
|
ENST00000319562.10:c.620C>G
|
ENSP00000322926.6:p.Thr207Arg
|
|
ENST00000490389.1:n.493C>G
|
|
|
ENST00000593548.1:n.673C>G
|
|
|
ENST00000595380.5:n.381C>G
|
|
|
ENST00000595437.5:c.620C>G
|
ENSP00000471242.1:p.Thr207Arg
|
|
ENST00000596467.5:n.479C>G
|
|
|
ENST00000599040.5:c.-50C>G
|
ENSP00000469420.1:n.-50C>G
|
|
ENST00000601009.1:c.222C>G
|
|
|
ENST00000602263.5:n.776C>G
|
|
|
ENST00000627049.2:c.620C>G
|
ENSP00000486285.1:p.Thr207Arg
|
|
NM_001286839.1:c.620C>G
|
NP_001273768.1:p.Thr207Arg
|
|
NM_005766.3:c.620C>G
|
NP_005757.1:p.Thr207Arg
|
|
XM_011521046.1:c.620C>G
|
XP_011519348.1:p.Thr207Arg
|
|
XM_011521046.2:c.620C>G
|
XP_011519348.1:p.Thr207Arg
|
|
XM_017020312.1:c.620C>G
|
XP_016875801.1:p.Thr207Arg
|
|
XM_017020313.2:c.467C>G
|
XP_016875802.1:p.Thr156Arg
|
|
NM_001286839.2:c.620C>G
|
NP_001273768.1:p.Thr207Arg
|
|
NM_005766.4:c.620C>G
MANE Select
|
NP_005757.1:p.Thr207Arg
|
|